Tag | Content |
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EnhancerAtlas ID | HS052-02538 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:156065430-156068150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr1:156066188-156066199 | TGTTGTGCAAT | - | 6.14 | CTCF | MA0139.1 | chr1:156066570-156066589 | GGGCCAGCAGGTGGCGCCA | + | 7.82 | NR2C2 | MA0504.1 | chr1:156065864-156065879 | TGACCTCTGACCCAA | - | 6.32 | NR2C2 | MA0504.1 | chr1:156065510-156065525 | GGGGGTTAGAGGTCA | + | 6.51 | NR2F1 | MA0017.2 | chr1:156065860-156065873 | CTTTTGACCTCTG | - | 6.59 | Nr2f6 | MA0677.1 | chr1:156065864-156065878 | TGACCTCTGACCCA | - | 6.37 | RFX1 | MA0509.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | - | 6.89 | RFX1 | MA0509.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | + | 6.91 | RFX2 | MA0600.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | - | 6.76 | RFX2 | MA0600.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | + | 6.88 | RFX5 | MA0510.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | - | 6.22 | RFX5 | MA0510.2 | chr1:156066986-156067002 | GGTTTCCATGACAACG | + | 6.3 | RREB1 | MA0073.1 | chr1:156067775-156067795 | CCACCCACCACCATCACCCC | + | 6.09 | Rxra | MA0512.2 | chr1:156065511-156065525 | GGGGTTAGAGGTCA | + | 6.09 | Rxra | MA0512.2 | chr1:156065864-156065878 | TGACCTCTGACCCA | - | 6.12 | TBX21 | MA0690.1 | chr1:156068038-156068048 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:156068038-156068049 | AAGGTGTGAAA | + | 6.62 |
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| Number of super-enhancer constituents: 45 | ID | Coordinate | Tissue/cell |
SE_00096 | chr1:156065452-156068563 | Adipose_Nuclei | SE_01581 | chr1:156065560-156068296 | Aorta | SE_02264 | chr1:156065996-156067725 | Astrocytes | SE_04119 | chr1:156066419-156067747 | Brain_Anterior_Caudate | SE_05125 | chr1:156065563-156067404 | Brain_Cingulate_Gyrus | SE_05929 | chr1:156065385-156069202 | Brain_Hippocampus_Middle | SE_08091 | chr1:156066374-156068302 | Brain_Inferior_Temporal_Lobe | SE_12411 | chr1:156066236-156067919 | CD3 | SE_13990 | chr1:156066343-156067150 | CD34_Primary_RO01536 | SE_14505 | chr1:156065871-156068273 | CD4_Memory_Primary_7pool | SE_16807 | chr1:156065659-156067859 | CD4_Naive_Primary_8pool | SE_17218 | chr1:156065550-156068458 | CD4p_CD225int_CD127p_Tmem | SE_17950 | chr1:156065300-156069187 | CD4p_CD25-_CD45ROp_Memory | SE_19616 | chr1:156065431-156069425 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20836 | chr1:156065575-156067852 | CD8_Memory_7pool | SE_23093 | chr1:156065378-156066171 | Colon_Crypt_1 | SE_25840 | chr1:156065674-156068547 | Duodenum_Smooth_Muscle | SE_26548 | chr1:156065336-156068204 | Esophagus | SE_27785 | chr1:156066105-156067222 | Fetal_Intestine | SE_28870 | chr1:156066270-156067179 | Fetal_Intestine_Large | SE_29555 | chr1:156065372-156068015 | Fetal_Muscle | SE_31480 | chr1:156066184-156067846 | Gastric | SE_34290 | chr1:156065319-156067522 | HCT-116 | SE_34622 | chr1:156065156-156067691 | HeLa | SE_35870 | chr1:156065471-156067456 | HMEC | SE_36976 | chr1:156065737-156067519 | HSMMtube | SE_37998 | chr1:156065282-156068432 | HUVEC | SE_40679 | chr1:156065452-156067998 | Left_Ventricle | SE_42123 | chr1:156065499-156068113 | Lung | SE_44150 | chr1:156065487-156068218 | NHDF-Ad | SE_44752 | chr1:156066014-156067478 | NHLF | SE_45674 | chr1:156065383-156068099 | Osteoblasts | SE_46650 | chr1:156066459-156067742 | Ovary | SE_47353 | chr1:156066082-156067442 | Panc1 | SE_48596 | chr1:156065694-156067966 | Right_Atrium | SE_50099 | chr1:156065286-156067986 | Sigmoid_Colon | SE_51113 | chr1:156065341-156068292 | Skeletal_Muscle | SE_52395 | chr1:156066354-156068063 | Small_Intestine | SE_53563 | chr1:156065686-156068198 | Spleen | SE_54528 | chr1:156065632-156069193 | Stomach_Smooth_Muscle | SE_55941 | chr1:156065931-156068449 | u87 | SE_63596 | chr1:156066572-156067180 | HSMM | SE_64308 | chr1:156065447-156067140 | NHEK | SE_65290 | chr1:156066034-156067742 | Pancreatic_islets | SE_67798 | chr1:156065931-156068449 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 156065683 | 156067549 | chr1 | 156066868 | 156067143 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I156095 | chr1 | 156065334 | 156069110 |
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Enhancer Sequence | AGCCACTGCG CCCGGTGTCC AAGACACTTC TAACGCCAAC ATCCTTGTAC TAGGCCCTCT 60 TCCAGCTCCC CCAGGAGTCT GGGGGTTAGA GGTCAGGCTG CTCCCCACTC TATTACCTCC 120 CCACACTTCT AATTAATTCT TGTGTTCAGT CCCAGAACCT GGAGAGTTAC ACTCAGGCTG 180 CCTGGTCCTG CTTATTGCCC ATATCCTAGA GGCACTTGCA TGCCCTTCCA GGCGGGTAAC 240 TGTACATGTC TCTCCCAGGC AGCCTTCACA GACTACTCAG GGGTATGGAT TGGCTCCAGC 300 TCTGACACTC AGACCTGAGC AGAGGCGTGA TCTACTCTGG CCTCCTGTGT TTCTGTGCCC 360 CACCTTCCCA CACTGCCCAG GGCTCCCTGA GAGTGATGCT GAGTCTAGTC TCAGCTTTTA 420 TGTTGCTTTG CTTTTGACCT CTGACCCAAC ACATGCCTCC TTTCCCTCTG AAGTCTTGAT 480 TTTCTCCCTG GCTTTTCTCC ACCTTCTGGG TGTTCCTTTT TGGCCTTCTT TGCCCATCTC 540 TCCTCCTCTG TCTACACAGC CAGGGGCTCC CCCTTCCGTT TCCTCTGCCT GGAACACACT 600 TGCTTCTCCC TTTCTGACTG GCTATTCAAG CAGGATCCTG TAGGTGGGTG GCAGTGCACT 660 GTGTATTACC TGTGAGCCCT ATGCAAATTA CCGCACATCT CTGAACCTGT TTTCCCATCT 720 ATAAAGTGAA GCTAATAGTA GCAATTACCT CATGGGATTG TTGTGCAATT AGTGGGAAGA 780 GGCATGTAAA GTACTGACAT ACTGTCTAGT ACACAGAAAG TGCTTAATAA ATGTTGGTGA 840 TTATTATCCA GGACTCAGCT TAATCATCCC TTCCTCAGGC AGGCCTGCCA CACAACCGCA 900 GACCGGGTTA GGTGCCGGGT TTTCTGCTCC CCAGCGTTTG GAGGCACTCA TCACACATTA 960 ATTACTTTAT CCATGAAGAT GAAAGCTGTC TTTGGCACCC AGATGGTACT GAGTAAATAT 1020 CTGTGAATGA ATGAATGATG TGGAATGTCT CCTCTGGAAG GACACAGTCA GGGCCTCCTG 1080 CCACTCAGGA CTAGCCTGGA TGCACCCACA GGGAAGGAGA AGGTGGGGCT GGTCTCCGCT 1140 GGGCCAGCAG GTGGCGCCAG GGCCTGTCGG TCTCTCCCCT TGGCCACCTC CCTTGCGCTT 1200 GCTCATCTCA TGCCCAGGCG CTGAGGGTTC TCAGCTGGGG CAGGAGAGAT GGGGTCCTGA 1260 GGCCTGGGTG AAGTTCCAAG CCCTGGGGCT CGGGGGCAGA CTCTCGCTCA CCCCTCCCAG 1320 AAAGATGTTT TCCTAGGGGA TGTCCAGCCT AACACGGCAG GGAAGGAAGT GGTGGTCACC 1380 TGGGAAAGGG GCCAACCTGA GAGGTTGGGG GTCCTGATGA GGCTGCTATT CTCTTGAGGA 1440 CATGAAATGA GAGGCGGTGA AGTCAGTCAG TGAGTCAAAA GCTGAGATCT AGGAACCAGA 1500 CACAATGTGG GAGAAGCTGC GGTGAAATCA ATCAGTGAGA GAGGAAGGGG AGGCCCGGTT 1560 TCCATGACAA CGGTAGTGTT TGTGGCAAGC TGGGGACTCC TGGGTCCCCA GGGCCCGCAA 1620 GCAGTGATTC ACCACAGGAA AGGGAAGGCT GCAGAGTGAC CTGGTGCTGG GGACCGGATG 1680 CCTTGTGGCT CCTTCTCACT GCTGAGCATG CATTCCCCCA GCCCAGGCCT TGGATCTCTG 1740 CTCTGCCAGC TACTGGCAGG GAAACTGAGG GATGGCAGAA CTGAGCCCCA ATAAGGGGCA 1800 GGCGCTTTGC TCCACGCCGT ACATGCACAT ATCACTTATA TCACTTATTG CTCACAACAG 1860 TCCTATGGAA TTACCGTTAT CCCTGTTTTA TCAAAGAGGA AACTCTCAGC CTGGCCCACG 1920 GTGCCATGGG CAGGACATGA GTGGCAGAGC CAGGATTGGA ACCCAGGCTA GCCTGACTCT 1980 TTACCATGCT TGGGAAGGCC CAGAAAGCAG AAAAGGAAGA GCAGGAGCAT GAGAGTTAGA 2040 GGATGGTTCA GACCCCAGAG GAGATGGACC CCAAGGCCCC TAGCCTCCCT GCCTGCCCTG 2100 CCCTATGCGA GCCCAACACT GATACGGAGG AAAGCTGGCC AACTGCATGG CCTAATGTGG 2160 GCCAGAACCT GGGCAGCCAG CCTACCTCTC ACTCTCCTCC AAGCCCAAGA GAGTAGGCCC 2220 CAGTTCCAGT CCATCCAACT GGATGGTAGC TCCCCCACCG TTTTCTCTCT GCCCTGGTCC 2280 TAGGGGCAGG GGTGCGTGTG CGTGTGTGCG TGCGTGTGTG TGTGTGTGTG ATCATCATGT 2340 CTACACCACC CACCACCATC ACCCCTATCC TCCAGCTTCT GCTATAGCCT GGGAGTTCCC 2400 AGCCTTTTAG TCCCTGTCAG GATAGTTTCA TTCTTGTTCA GCTTTGGGGC CCACACAATT 2460 TCAGTACAAA AGGGGTATGC CCATCTCACC CTGGGCCTTG ATAGCATGCA AGAGCATAGT 2520 TCAGGCCCTC ATCATCTATT CCCTTGTAGT AGAAGGGATG GAGGTTGGAA AGACCTTAGA 2580 AATCTTCCAG TCTGGTTCTC TTGTTTTGAA GGTGTGAAAG CTGAGGCTCA TAGAAGGGGA 2640 GCAATTTTTC TGAGGTCACA GAGCAAGTTA ATGGAAGAGT GAACTAGATT CCCTGTCCAC 2700 AGACTTCAGG TTCTGTAATC 2720
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