Tag | Content |
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EnhancerAtlas ID | HS091-30554 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:31766380-31767400 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr20:31767019-31767034 | GAGGTCAGGAGTTCA | + | 6.22 | TFAP2C | MA0524.2 | chr20:31766763-31766775 | TGCCTCAGGGCA | + | 6.18 |
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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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Enhancer Sequence | GAAAATTAAT ATCACATATC ATACAATCAA TGGACTTATA AAATAGTTTT AATTTTTTTT 60 CCATCTGTGC ATCATCCAAA ACCATAGGTA CCATGTGCAG GATTACTAGG CCCAAAGTTG 120 CAGAGATTCT AAATCAGTCA TTCTGGAAGC AGACCCAGGA ATGTGGGTTT ATAAAAGAAA 180 AATCCTCCGG ATGGCTCTGT GACCCACTGA ACCGGAGTTT AGTTATATTC CAAAAGCGAT 240 CCTCCACCAG CTTCAGCCTC AGCTGGGTGC TTGATAGGAA TGCGGAATCT CAGGCCACAC 300 CCCAGACCTG CTGAATTGCA ATCTGCGGGG AACTGTGTAC ACACAGGAGC AAGAGATACT 360 CCGCTCTACA ACCTCAGGGC AAATGCCTCA GGGCACCATT TGACCCTTTA AAATTCCAGG 420 GTTCCAAAGT TCAACATGGG AATGTTAACA ATCTAGAATG TAGATTTTTG AGGTCCTAGA 480 ATTCTAGTGT TCTAAGGTGT TAGGATTCTA ACACCCTAGG GTTTCCAGAT TTAAGACTGC 540 TGGGATCCCA TTGTTCTAAA ATCCTAAGGT TCAGGCCAGG CGCGGTGGCT TATGCCTGTA 600 ATCCCAGCTC TTTTGAAGGT CAAGGTGGGC AGATCACTTG AGGTCAGGAG TTCAAGACCA 660 GCCTGGCTAA CATGGTGAAA CCCTGTCTCT ACTGAAAATA CAAAAATTAG CCAGGCATGG 720 TGGCATGTGC CTGTGAACCC AGTTTCTTGA GAGGCTGAGG CAGGAGAATC ACTTGAATCT 780 GGGAGGCGGA GGTTGCAGTG AGCAGAAATC GTACCACTGT ACTCCAGCCT GGGCAAGACA 840 GTGAGATTCT GTCTCAGAAA AAAAAAAAAA AATACAATAA AACAAAATAA AATCCTAAGG 900 TTCAAAGATT CTAAGATCCC TAGAAATGAG CTCATCTGTG GGTGGCAAGC AATTTGTTCT 960 CAGCTGAGAA GAATGATCTG TTCTTCCTCC TACTCCTGAC CCTCCTCTTC CTCCTTTCTC 1020
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