Tag | Content |
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EnhancerAtlas ID | HS116-05885 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:11589400-11590730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr11:11590290-11590305 | GGGCCTGGGTGACCT | - | 6.26 | RREB1 | MA0073.1 | chr11:11589419-11589439 | CCACCAATCACCCCAAAACA | + | 6.77 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_02148 | chr11:11589430-11590711 | Aorta |
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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 |
GH11I011567 | chr11 | 11588902 | 11592722 |
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Enhancer Sequence | TAAACATCCT ATATATCTTC CACCAATCAC CCCAAAACAC CCATTCTGGT ACAATGCATT 60 CGTTAACAGT TACCACCCTC ACCCTGTCTT TAAGAGAACT ATATAACCCA TCTCCCTTGC 120 CTTGTGACTC ACAAAGGCCT GGCCCCACTG CCAGGCATTG CCACGTGACT GATTTTGGCC 180 AACAGAGTGT GAGCAGACAT GAAGGATGCC AGGTCTGAAC AGAAGTTGTA AATGTGACTA 240 TACAATTTGG CTCAGCCTCT TGCTGTTCTC AACCACAATA AAACAGGCAG ATCACAAAAC 300 GAGAAAGTAT GTGGAGCAGA ACCACAGCCA ACGCACAGCC CAGGTGACAT AAGGAAGAAA 360 GAAACTGTTG CTTTGTAAGC CACTGAGAGT TGAGGTTGTT TGTTATGCAG CCAGACTTCG 420 CGACAACTGA CTAATTACCC TTCAATACAG GAGTAGCAGG TAGCTCTGGG GAGTTGGCCA 480 GCTCTTTGCA CCTATGTCCT GTGGCTCCTA TCACCCACCT AACAAAGCCC AGGCCTAGTT 540 CCAATTTCAC CATAACTCAT TTTCCATCCA TTTATACCCT AGGCTCCTTA AGAAGTGAAT 600 CTTCCCGGCA ACACCCTTAG TTCATGACTC ATCCTGCCAG TGACTCTGGT TAAGGGGGGA 660 AAAAGGTAGG TTTAATGTTT CAGCAACGCC ACTGGAGATC TCAGAGTAAA AATCACCCCC 720 TTTTCCTCTC CTGGGGAGGC TCCACACCAA GAGCCAATGG AGACTCACTG TCTAAGATAG 780 AGAGCAAGAT GTACAGGAGA GGGCACTGGA CTAGGAGTCT GGAGTTCTGG ATTTGGATTC 840 AGGCTAAGTC ACTGGGCCAT GTGACCCCCT TAAAACCACG GAGTCTCTAA GGGCCTGGGT 900 GACCTAGTAC AAGTCATTCC CTCTGTCTAA ACTGATCAGT GGTTTTCAAA CCCAGCATTG 960 GTTTCCTTGG AGATGTCTTA GCCGATAGCT GAGATGAGAA GAAGCCTGTG GCCAATATAA 1020 CCTCATCCCC TGCTTCTGCC AGATGGGCTC TGTTTTGATC TACTGTACAA ATTCGGTTTC 1080 TAGGTAAGAT GTTGCTTAGC CAAGAATCCC ATAGCTAAAT GCATTTCAAA ATCACTGATC 1140 AGGTGATCTC TGAGGGCCTT TCCAGATCTG ACACATGCTG ATCCTCCCTG ATGCCTGACT 1200 TCTTGTATAT TCTGTGGCCA CCCACTTCCT TGCCATTGTA GTCAAGGATT TACTAACACC 1260 CAGAGGGCAC CCAGTAGTGA ATGACTGACA AGCAAGAATG TAACAAGGTA GATTCACAAC 1320 AACTCAACCA 1330
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