Tag | Content |
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EnhancerAtlas ID | HS095-24815 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:141432700-141433720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr5:141432823-141432836 | ATATGCAAATTAA | - | 7.34 | Pou2f3 | MA0627.1 | chr5:141432821-141432837 | ACATATGCAAATTAAA | + | 6.42 |
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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 |
GH05I142052 | chr5 | 141432394 | 141433764 |
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Enhancer Sequence | AGCCTAGGTG ACAGAGTGAG ACCCTGTTTA AAAAAAAAAG AAAAAAATTG AAGTAGAAAG 60 GATATTAAAA TATGACACTG AAGCTTAGGC AACACCAAAG AAAAGACTGA TAGACGTGAT 120 TACATATGCA AATTAAATAC TTCAGAAGAG AAAAAAACAA GTCAAAAGAC AAATGAAAAC 180 TGAAGAGAAA TATTTGCAAC CTATAAGACA GACAAGAACT AAACCCTTAA ATAAAGAACT 240 TTTACAATTT CATGCAAAAA CAACAACAAC AAAAGGACTC CAAAACATGT CCCAGCAGTA 300 TGTCTCCTTC CCTGGGTAAC TAGATTGTAA CTGTGGAAGA CAGCATTGTG TCTGAAATGT 360 CTTCCTACTG CTCACAGAAT GTTACACATT GTCAGTACTC AGATCGAGTC TGTTGATTGC 420 AGCTCTTTAT ACCACTTCCA AAAATTCCTG TGCTTGTTTC TGTTCCTCCC CTCAAGTACT 480 CTCCTCTTGT CTCTCTCAGA GCAATGTCAT TAAGATGCTT CCTGTGCAAT CTGTGACTCA 540 CAGCTAGATT ATGGCACAGG CAGTGCTGAT TTCAGCAAGA AACTGTCCCC AAGGCATAGA 600 TTGCGTTCCT GCAATGATGC CCAAAGAGAA AATTAAAACA GGAAAGTCTT TGCATTCATT 660 CAGCACCTCA TTCTTAGACC CTTACTATGT ATCTGGAGCT GTATTTTTTA TCTGAGTTGG 720 TGCTCATGAG GGAGAGTGCA GCCAAGAGAC CTGGTCGGGG GGAAAGGATG CTGGGCCAGG 780 AGATCTGGAT ATAAGTGCTG GCTCTGCCGC CTGTGCTCTG GAGGACCAGA TGGGTCCCTT 840 CCAGCACTTG GCCTCAGTTT CTCCCTCTGT AGAACAACTG AGGGAACTAA GTGGTCCCAT 900 GGGCTCCTCC AGCTCTGACA TCTGAGGATT CAGCTCATTT CCTCTTTTTA AAGTGTAGAC 960 TCTAATATCT GGTTTAATCA TAATTGAGAA GTGTTTTGAA GTCCCTTAAG AGTCCTTGTC 1020
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