Tag | Content |
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EnhancerAtlas ID | HS095-23661 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:17154310-17155720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr5:17155017-17155030 | TTCTGGAACTTTC | + | 6.32 | Nfe2l2 | MA0150.2 | chr5:17154911-17154926 | CAGCTTGACTCAGCA | + | 6 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56046 | chr5:17154093-17160334 | u87 |
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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 |
GH05I017154 | chr5 | 17154255 | 17155403 |
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Enhancer Sequence | AAAAAGCAGG TGACAGTCTG GCCAGAGTAG AGGGCATAGA AGTAGAGGCT GCCATGCAGA 60 TATCAGGCTA CATTGACAGC ATCCACTTCA CCTGTCAATT CAGCTTTCTT AACCTGCCTT 120 CCCCTAAACA TGCTTTTTGT CTTTATCGTG GTCTCTAATC CCTTGACTTA TCTATTTGCA 180 GCTAATTATC AGCCTCCTGG GGACAATTCC TTCCATATGG AGCCTGGCTC TCAGAGACAA 240 TTAGCACCTC TTCCTCTCAG GCTACTCAAC TTCATTGTCT CCTTGTGTTT TTTATTTTTT 300 CCTTTTTTTT TTTAACCACA ACTTGGTGTT TCCCAGCTAA ATTCAGACTA TGATAACTAG 360 AAAGAATTGC CCACCCAGGC AAACTGGTGC CACCGAAAAT TAATGGAAAT CTCTCTCCTC 420 GGTTTATTTA TTTATTTTGC ATTCTTTTTG GTCAGGTCTT CCTTTAGTAA CTCTCAGCTA 480 CAAGTCTGAA CTTTTGCTCC TTCCTCAAAT CACCTTCCTG ATTTTACTGC TTTTATTCAT 540 AGTCAATGAC TCAGTCATTC TGGATCTAGA TAGAATTGTC TACACTCACT GTCTCATTCT 600 TCAGCTTGAC TCAGCATGAC TTCTGGCTCC ATTACTCTTC CACGTCAATC CAATGGACTT 660 TTCTACTCTC ACCTTTCTTC TTAGCAACAT TCTTGAACAT GTCCTCTTTC TGGAACTTTC 720 TTGCCCCCAT TTTCTGACCG TAAAGCTATC TTAGTTTTCT TCTGAACTTC CTGGTCATTT 780 CTTCTTTCCT TTTGCAGTTT CATCATCTTC TATCTAGCCA CTGATTCTTT GAGCTCCTCA 840 AGAGTCTGTC TTGGCACCTC TCCTTTCCTC CATGTTCTGT CCATAAACAA TCTTATCCTA 900 TCTATGCCTA CTCTTCATAT CAATAATTTG GGCTTCTCCT TTGAGATCTA GTCTTACCTG 960 GCCAACAGTC TACTTGATAT CCACTCTTGA ATGTCCCAAA GGCACATTAA AATCAATATA 1020 TCTAGAAGTA AATGCATGAT CTTCCTTCGA AATCCAGGCT GCTTCCAGTG TACTTCATCC 1080 TGGTAATCTA CCCAATTTGG GGCAGATCCT AAATGTAGGG GGCCAGCCTC AATATTCCTT 1140 CACCTTACCC TTACTGAATT TCAATAATAT CTTTCTAAAT ATCTTTTAAA GTTATCTTCT 1200 TTTTCAATTC TCACCACTGT CACCTTTTTT GAGCTATAGT CATCTCTTTC CAGGGTTACC 1260 AAAGTAGCCT CACTAGCTTA TTTTGTCCCC TCTGGATTCC TCTGGTCCAT TCTCCAGGCT 1320 GCGGCTAAAG TCAACTTTTG AAAATGTATA AAATACAAAT GTGATCATGT GAGCTCAGCC 1380 ACCTATGCTT TTTAAAACTC ATCAATGACT 1410
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