Tag | Content |
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EnhancerAtlas ID | HS131-00872 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr1:235146990-235149540 |
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) |
RREB1 | MA0073.1 | chr1:235147328-235147348 | CCCCCACACACACCCACGCC | + | 6.07 | ZNF263 | MA0528.1 | chr1:235147070-235147091 | TTTTCCTCTCTCACCTCCCCC | - | 6.41 | ZNF263 | MA0528.1 | chr1:235148891-235148912 | GAAGAAGGGCGGGGGAGAGGA | + | 6.65 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_02305 | chr1:235147035-235148901 | Astrocytes | SE_06052 | chr1:235147258-235149727 | Brain_Hippocampus_Middle | SE_25800 | chr1:235146945-235149402 | Duodenum_Smooth_Muscle | SE_26806 | chr1:235147079-235148893 | Esophagus | SE_29689 | chr1:235147728-235149217 | Fetal_Muscle | SE_31235 | chr1:235146510-235149391 | Fetal_Thymus | SE_32614 | chr1:235140175-235154143 | GM12878 | SE_33758 | chr1:235147075-235148879 | HCC1954 | SE_34767 | chr1:235147005-235148891 | HeLa | SE_36058 | chr1:235146614-235149471 | HMEC | SE_36952 | chr1:235146938-235152568 | HSMMtube | SE_37966 | chr1:235146872-235149155 | HUVEC | SE_40653 | chr1:235147027-235149414 | Left_Ventricle | SE_42265 | chr1:235147105-235148992 | Lung | SE_44202 | chr1:235146927-235148930 | NHDF-Ad | SE_45558 | chr1:235146593-235149758 | Osteoblasts | SE_47119 | chr1:235148155-235149767 | Panc1 | SE_50071 | chr1:235146899-235149198 | Sigmoid_Colon | SE_51271 | chr1:235147542-235149156 | Skeletal_Muscle | SE_52352 | chr1:235147001-235149055 | Small_Intestine | SE_53330 | chr1:235146848-235149167 | Spleen | SE_56068 | chr1:235146597-235149251 | u87 | SE_57395 | chr1:235146972-235147669 | VACO_503 | SE_59274 | chr1:235138265-235187641 | Ly3 | SE_60969 | chr1:235059965-235155853 | HBL1 | SE_62329 | chr1:235047040-235185428 | Tonsil | SE_63542 | chr1:235146861-235147654 | HSMM | SE_63542 | chr1:235147688-235148831 | HSMM | SE_65393 | chr1:235146807-235149156 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I235010 | chr1 | 235145789 | 235150146 |
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Enhancer Sequence | ATCAAGCCGG GGCTTTTAGT CAACTCTCCC ATGGGGACTC TGTTGGCCCG CTCCACCTCG 60 GGTGTTCCCC CGCCCCTGCC TTTTCCTCTC TCACCTCCCC CATCCACCCC TCTCAGCCTT 120 GCAGTCGACC TGCCTCTCCT CTGGTTGCTC CGTTTGTAGG GAGGGTCTGC TTGAAGGGAG 180 TTCCCATTCT CTCTCACCCA GAGTCAAGGC TCTTGACTCT ATTGTACCTA AAAAGCTCCT 240 GAGGAATTTG ACAAGGCCCC ACCCTCAGAG ATATGGGGTG AAGCCCAGGA ATCTGTATTT 300 TTAACAAGCA TCCCAGGTGA TCCTGATACT TGCACACACC CCCACACACA CCCACGCCGA 360 CTACCCACAC ACTTCCATGG CCCAGAAGTC TGCAGGACCC ACAGCAGGTA TTCGGGACTA 420 TTTGTTCAAT CCACACCTGA GTCGTTGCAC GATTATGCTC AAGTCCCTCG GAACACCTCG 480 CCTGCCATCT GACAGCTTCC CATCCAGAAA CCACACAGTA CAGTAAAAAA CAGAAAAAAG 540 AAAGCCGTTA GACCCCAGTG AATGTTATTT TTAATGAAAG TGGTGCATTT TGACTCACAA 600 TGTTGAAACC AGATTATAAA TGAGTCATCA GTGAATCGAC CACAAAGAGC CTTTGCGGAG 660 GTGATTTACA GGAGAGCTCT GATGTCTGCT GTCCCCTGCA CACGCTTCAC AGAGATGCTG 720 TCAGACGCAG AGCTGGTCTG GGGCATCTGT TGCCGCGTCA GCTCAAAAGG ATGCTGTGTT 780 GTCACCAATG GGATTCCCCA GCCCAGGCGG TGTTGCGGTC CCACCCACAC AAGGAAGGCG 840 GCCATCACTG AATAATGCTT GTGGTTACAT CATCATTGCT GGTTTCCAGG TAGTGACTAG 900 CAGATACTGG AGAGAGACAG GCCATCTGCT CTTCCTGTGC GCCTCAGCTC CTCCCTCATA 960 CCCACATCCT CTCGCCTGGT CTTCTAGAAG CAGCCCCTAT GCAGACAGAC CAGCAGGACT 1020 GAAAGCTGGA CAGACTCGAG CCGGAGAGCC AGGTGGAACA ACCTGGCCAG AAAGAGTCTG 1080 GCCGCAAAGA GTCTGGCCAC AGCCCCACTT TCCTCATCTC TAAAATGTCC ACATGGCTGC 1140 CTGCCCTGCC CGGCTCAAGG GAATGTTGCA AGGCTCTCAT GGAAACCATG CTTGTGAGGG 1200 TTTTGAGGAC TATCATAGCC CGTCCCAAGG TCAGAGGACA GTAGAAAACA AAAAACTTGC 1260 TTTCAGAGGG TGCTTTCACC AGTCAGCAGC CTCTGCCCCG GGCAAAGCCA GACAACTAAA 1320 ACGGAATGAA TCCGCAGAGT AGGGTGGGGA TGAAATTCTC CACCTCCAAC CCAGAAAGGA 1380 AACGCCAATG CTCATGTTTC CCCTTAGAGA AACAGGCAAT GTTTGAACAG GAACAACGAC 1440 GCCAGAGGGT CAATCCACAC ACAGAACACT CCATCTCCAT GCCGATGGGG GACTGACTGT 1500 CCTGCTGCTG AACTGCACCC CTGGGGCTCT CCAGGACACT CCACTGGTGG CCACACTCAG 1560 GAAAATAAAG AAAAACCTTC AAAAGGACCC TTCTGGCCAT TCAGAGAATG CACAGGCCTG 1620 CTAGCTCCTG CTTGCCTGCT CAGAGCTGCC TCCACTGGGG CAGGAATCTG CAGCCAAGAA 1680 AATCCCTGAC AACCCCAGGG ACAGAAGGGT CAGTCTGGGG GACCATCGAC CAACCCAGCA 1740 ACCCAGATTA GACTGCTCCA CCAGGAACTC TGTGTCCAGA GAGCAGGATC TGCCACAAGC 1800 AAAACTAGGC CTCATTTACT ATTCCACAAT AGCAACTAGA AAGCATGTGA CCCAGAAAAC 1860 CTTCAAAGAA GGCCAGAAAT TCATTAAATC TGAAAAGAAG GGAAGAAGGG CGGGGGAGAG 1920 GAAAACACTG CTTAGCAAAG CCAACTGAAT CCCTCTTCCA TACATCACAG ATGCAGGACC 1980 AGTCTCAGCA TTCAAGAGGA AGAGAAAAAT GAAAACAAAA ACCAATCTGG AGTTGAATGT 2040 CAGCCTTCCC CTCACTGGTT CTGGGTCCTT TGGAAGGCCA TATTGTCCCC GGACCTCTCT 2100 TGCTTCAGTG GCCTTCCTGC CAGGATTGCC ATAAGGATTA AATGGACTCA TATATGTGTT 2160 GTACCTATAC AGTACCTGCA ACACAGTAAA TATCCAATAA ATGTTGGTTT CTTGCTACAA 2220 GAAATTGTAA AATATGGGCA CAAATTCCTC CTACTTTGTT AAGCACATCC CTTGGCAATG 2280 ACTTAGCTGC TACTCCCATC AAGAGTTGTG GTCTATGTCC CTACCCCTTG AATCTGGGCT 2340 AGCCTGGGAC TTGCCTCAAC CAGTAGAATT TAACAAAAGT TACAGTGTGT GACTTCCAAG 2400 GCTAGCCCTT GCCGCTTCCA CTTTTGCCCT CTTGGAATGT GGCCCAGAGA CAACCATCTA 2460 AGGAAGCTGA TCTAGGCCAC TGGAAGAGGG GTGGGCAGAT GGAGAAGTGA TGTCCCCCAA 2520 CCAGCTGCCA GTCACATGAG AGAGGCCATC 2550
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