Tag | Content |
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EnhancerAtlas ID | HS098-04806 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:207997120-208000640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr1:207999927-207999938 | ATGTTTACTTA | - | 6.02 | Foxa2 | MA0047.2 | chr1:207999928-207999940 | TGTTTACTTAGC | + | 6.52 | HNF4G | MA0484.1 | chr1:208000278-208000293 | TGAACTTTGACCCGC | - | 6.08 | Hnf4a | MA0114.3 | chr1:208000276-208000292 | GCTGAACTTTGACCCG | - | 6.87 | IRF1 | MA0050.2 | chr1:207999508-207999529 | GTTTCCTTTCATTTTCCCTCT | + | 6.71 | IRF2 | MA0051.1 | chr1:207999507-207999525 | TGTTTCCTTTCATTTTCC | - | 6.49 | NFE2L1 | MA0089.2 | chr1:207998147-207998162 | GTTGCTGAGTCATTT | - | 6.77 | NR2C2 | MA0504.1 | chr1:208000278-208000293 | TGAACTTTGACCCGC | - | 6.11 | Nfe2l2 | MA0150.2 | chr1:207998149-207998164 | TGCTGAGTCATTTGT | - | 6.25 | Nr2f6 | MA0677.1 | chr1:208000278-208000292 | TGAACTTTGACCCG | - | 6.22 | RREB1 | MA0073.1 | chr1:207997136-207997156 | CCCCCCACCACCACCCCACC | + | 8 | Rxra | MA0512.2 | chr1:208000278-208000292 | TGAACTTTGACCCG | - | 6.92 | SREBF2 | MA0596.1 | chr1:207999211-207999221 | ATCACCCCAT | - | 6.02 | Stat4 | MA0518.1 | chr1:207998346-207998360 | CTTCCAGGAAGGGG | + | 6.29 | TBX21 | MA0690.1 | chr1:207998903-207998913 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr1:207998902-207998913 | ATTCACACCTT | - | 6.02 | TP63 | MA0525.2 | chr1:207997738-207997756 | TAAATGTTGCAACATGTT | - | 6.58 |
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| Number of super-enhancer constituents: 48 | ID | Coordinate | Tissue/cell |
SE_00306 | chr1:207977138-208002770 | Adipose_Nuclei | SE_01416 | chr1:207993530-208001102 | Adrenal_Gland | SE_01610 | chr1:207977672-208001114 | Aorta | SE_02940 | chr1:207994764-208001210 | Bladder | SE_03274 | chr1:207994642-208001056 | Brain_Angular_Gyrus | SE_03907 | chr1:207991667-208003388 | Brain_Anterior_Caudate | SE_06993 | chr1:207991689-208002991 | Brain_Hippocampus_Middle_150 | SE_08580 | chr1:207991706-208006704 | Brain_Inferior_Temporal_Lobe | SE_08815 | chr1:207997399-207998065 | Brain_Mid_Frontal_Lobe | SE_08815 | chr1:207998353-207998830 | Brain_Mid_Frontal_Lobe | SE_09440 | chr1:207995744-208003407 | CD14 | SE_10475 | chr1:207994104-208000942 | CD19_Primary | SE_11488 | chr1:207992533-208010277 | CD20 | SE_12401 | chr1:207995997-208000598 | CD3 | SE_13353 | chr1:207996071-208001084 | CD34_Primary_RO01536 | SE_14644 | chr1:207995084-208002663 | CD4_Memory_Primary_7pool | SE_17929 | chr1:207994596-208002969 | CD4p_CD25-_CD45ROp_Memory | SE_18828 | chr1:207994794-208013240 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20606 | chr1:207994659-208001166 | CD56 | SE_21313 | chr1:207995382-208000901 | CD8_Memory_7pool | SE_21874 | chr1:207995258-208000511 | CD8_Naive_7pool | SE_23628 | chr1:207994832-207998453 | Colon_Crypt_1 | SE_23628 | chr1:207998491-208001207 | Colon_Crypt_1 | SE_24155 | chr1:207994777-207997940 | Colon_Crypt_2 | SE_24155 | chr1:207998106-207998462 | Colon_Crypt_2 | SE_24155 | chr1:207998607-208001173 | Colon_Crypt_2 | SE_25829 | chr1:207992121-208003797 | Duodenum_Smooth_Muscle | SE_26666 | chr1:207993695-208001206 | Esophagus | SE_31608 | chr1:207984660-208002274 | Gastric | SE_40741 | chr1:207976619-208001249 | Left_Ventricle | SE_41597 | chr1:207996136-207997919 | LNCaP | SE_41597 | chr1:207997975-208001110 | LNCaP | SE_42138 | chr1:207976803-208001181 | Lung | SE_45086 | chr1:207995936-208001117 | NHLF | SE_46988 | chr1:207996188-208000776 | Ovary | SE_48128 | chr1:207976505-208001203 | Psoas_Muscle | SE_48593 | chr1:207982190-208002314 | Right_Atrium | SE_49524 | chr1:207996226-207997869 | Right_Ventricle | SE_50299 | chr1:207993725-208002318 | Sigmoid_Colon | SE_51185 | chr1:207976162-208002674 | Skeletal_Muscle | SE_52485 | chr1:207994685-208001212 | Small_Intestine | SE_53314 | chr1:207993859-208001216 | Spleen | SE_54764 | chr1:207991828-208013085 | Stomach_Smooth_Muscle | SE_59011 | chr1:207980241-208007571 | Ly3 | SE_60122 | chr1:207993349-208003620 | Ly4 | SE_61319 | chr1:207994376-208006461 | HBL1 | SE_62794 | chr1:207980098-208006634 | Tonsil | SE_65312 | chr1:207986337-208001141 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 207999163 | 207999611 | chr1 | 207997315 | 207997832 |
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Enhancer Sequence | CTTGCTCCCA CCCCTGCCCC CCACCACCAC CCCACCTCCT CCCCACGGGA ACCGCCCGTG 60 CCACCTTGCG TGTCATCTCC TAGCCTAGGC TACCCAGAGG CCTCTGGCCC TGACAGATCT 120 CTGAACGCTC AGCAAGTGAG CTGGCAGAAC CTGGTGCCCG GTGTTGCTAT GACTTGTTTC 180 TTGATTTCTC TCTCTCTCTC TGCTGCAGCA CGGCTGTTGC TAGCAGACCT ATCGACGGAG 240 CTTGCTTGCT CGCTCGCTCT CTCACTCTCT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCA 300 GCTCTGTGAC GCAGATCTAA ATTCTCCAGT CTGCTCCTTG TGTTGCAAGA GCAGAACTGC 360 AGCTTTTCCC CTGGAGAGCC GGAGGGCAGT GCCAAGGCTG GTCAAACAAG GCAAAAAAAG 420 TTGGGCCTAC ACTCTGCTTC CTTGGCCACA CTTTTCAGCT CACACCCTCC CACCTCACCC 480 CTCCTGCACC TCACTGCTCT GGGGCATAGA GGTCCCTGTC CTTTCAGGCT CACTCCTTCC 540 CTGAGGCCTT CTCAGGCATA AGAGTAGCTT AACTCTTTGA GTGGCAGCCC CCAGTGCCCA 600 GACAGGGCTG CCCTGTACTA AATGTTGCAA CATGTTTTCT TGAGCCATAT GGGCTTCTCC 660 AGCCCTGAGA AAAAATGTTC CTCACCCTGA CCACTGTCCC ATTAACTCTT TGTGCCACAG 720 ACAAGTCCAG GATTACAGTC ATAGCTGATT TCTGTTGTTT TTTGCCTTTT TGGCCAAAAA 780 CCAGGACCTT TTTCTCCCTG GAATTTCTTA AGGACAAAAA GCGTAATTAA AACATTGCCT 840 GCCTACCCCA CACATGAGAT CCTTCTATCA GGGCAGGAAT TTGAAAAACC AAATTGAACT 900 GCAGCCTGAA GAATCCAGAG TAAAACCAGT CTGGATATCC ATCCTTCCTG GGCTCAAAAT 960 TTTAGGGCCT AGGTAAATAC GTTCAATTAC TTTTCAAGTA ATTGGCCACA CAGTCTCAGA 1020 GATTTGGGTT GCTGAGTCAT TTGTTCCCAA GAAGATCTGA CAACATGAAA AACAGCAAAA 1080 CAGAGCAACA GCCAAGCCTG GACCTGAAGT GGCCAATGAC TGGGTTCTCC TCTCCAGCAT 1140 GGGCAGTCAA GCAAGATGAG CATCCACGAG CCGACCCCCA ACCCCTCCAC AATGTTCATG 1200 CATGGATGTC CACACTCCTG GAAACTCTTC CAGGAAGGGG TGGTCCACCA ATGATCTAGA 1260 GATGGAGTGG GGTTGTTTTT GGATACTCAC AGGTCTCCAC TACAGCAAGC AAAGAGCCCC 1320 CAACATTTTC CTGCCCCTCC CCCCAGACGC AAAAATGCTT CCAAGAACAA CTGAGATACT 1380 AAATCACTAG ACCCTACATA CCCAGATAGA CCAAGGGAGT GTTGGGTTCC CACACTGCTA 1440 CATCCAAAGA ATGCAGAAAG GTTCCCGACA ACCAGTTGTA CCATATGAGC CTAGACTTGA 1500 CCAGAAGTGA GTGAGATATT CAGGTCCTGG GTCAGGTAAC TTATGAAGTC TATGACATCA 1560 AGAACCTTGC AACTTCCAGG AAGATGAATG AGAATGCGAG GCCAGGCAGC TACCTTATCC 1620 CATATCTGCT TCCCAGGCAG CCTTCTTCAA GCAACTACTC TGGGCCAAAG TTTCATCCGG 1680 CAGAAAGAAG GACCACTTGG AAGACAAGCA TGGCACTACA CAGTTTTAAA AGAAGACCAG 1740 AGTATCTGTG CCAGGCTCCC AGCAGGGGGG AAAGTGCTTC AAATTCACAC CTTCTGGGCT 1800 CCAAGGTTGA GCATGCCAAT AAAGAAGTTA CCTACTGGTC TGATGACCAA AGGAACGTGG 1860 CCTTGATGGC ACTAAAGCAA GTCCCCCAGA AAGGTCCTCT GGTTACTTAA ATCCCATTTG 1920 CCATAGTTTC CTTCTCCATG GAAGAAAAAC ATGCCTAAGT TCATGTCAGG ACATTCCTGA 1980 TTTATCCAAG AGCCCAGGAT CAAATAAACA AAGGGCTCTG AGCTCTGCCA GGGAGCCTCC 2040 TCCTTCAGGA GGCAGAACTA GAGGGAAGTA GGCTTGGTAC AGAGCTGGCC CATCACCCCA 2100 TGAACTTGGT GAGTGACGTG GCTGCTCACT GCCATGGCGA TGGGGATGTT ACGGGTGGGT 2160 GGAAGTGAGA GAAGAGGCAA ATAAGTCATG AGAGACGAAG CGAAAGCGAG GCAGGGTCAC 2220 AGGAGGAACC TACAAAGCCA CAGAATTTGT ACAGAGGCCG ACTGTAGTCT ATGACCGCAG 2280 CAAAACTAAG CTGAGTCCCT GCAAAGATAA GTCCCCATCT CAGGGGTGCG GCATGAACCA 2340 ACTATGACTC GCAAAAACCT ATGACAACAC TACGTTCAGC AAGGCTTTGT TTCCTTTCAT 2400 TTTCCCTCTA AATCTTTTCC TTCCCATGAC CCCGTTGGTA CGGCTTTGAT GACTGGAAGA 2460 ACACTAGGGT TTTCGGTTTT GCTCCGGTTT GAATAAAATG ACACAGACAT ACATGGAGTG 2520 GTTTTAAAGA GTGGAGAATT TAATAGGCAA GAAAGAAGGA AGAGGCTTTT CCTGTACAGA 2580 GACAGAGGGG GGCTTTAAGC CGAAAGAGGG AACCTTGAGT GCGGTGGAAA ACAGCCAGTT 2640 ATATGAGGAG GCTGGAGGAG GCAGGATTAA AACAGTCATT TTAGGTACCT CTGCCCAATT 2700 CTAGGTCTTC CTTCTATTAA CCTGATTCTA CAAGGCACCA AGAACAAAAA AACCCGAATG 2760 GGATGACCAG GAAGCAGAAA TGAATTCAGT TCCAAAAACA TGGGAGGATG TTTACTTAGC 2820 AAGCACGCTC GAGCCTACAA GGAAGCAGTT TTACAGGGTG CTGCATGCAG TGTTTGATTT 2880 CAGGGGGTAA AGATAACTTC AGAGTGGGGA AAAGGTGCTG GCTCCTTCTA CTCACCCTCA 2940 GAGGCTTGGG GAGGCCAGGC CAGCACAAAC TTGAAAAGGC AAGGCTTCAG CTCAAGCCCA 3000 ACAGGTTGCC GGCTCTCTTT GGCTCCTCGG CAGCTACCGG ACTCAGGAAC TAAACAAACT 3060 CTCCAGACTT CATGAGCATT CCGTGGCCTC CGACTGATCT GGGTCAAAAC TTCGAAATGC 3120 CAAAGACAAA GAATTTTTTT CTTTAAAGGG GAATGAGCTG AACTTTGACC CGCCCTTGTT 3180 CAGGGTGTGG AATGCAAGCA CTGTGTACCG GCCACAAACT CCAGTTCGGC AGGCAACAGC 3240 CAGAAAAGCA GTCTTCATGC CGGCTTCATG CCGGCCTCCC TGTCCTGTTT CCTCTTTAGG 3300 GCCAACTCGA CGGGGTCTAG GTCTTTACCT CGCTCTCCAG ACAGGGAAGC TGTGCAGAGG 3360 ACACATTCCA ATCTCTGTTA TCTAGAGCTA GAGTGGATGT TCTAGATAAA TCTGGCAGCG 3420 ATCTGGTCTC AGGTGGAACT GACAGGCCCA GTCCACAGCA AGATGGCATT TCTGTTCACT 3480 CCCTGGGAGC TGGTGGACAA CAGGCGCTTG GTTACCACCT 3520
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