Tag | Content |
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EnhancerAtlas ID | HS118-09994 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:65397420-65398470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr2:65397848-65397863 | GGTTAATGATTTATC | - | 6.67 | HNF1B | MA0153.2 | chr2:65397849-65397862 | GTTAATGATTTAT | + | 6.3 |
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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 |
GH02I065169 | chr2 | 65396521 | 65399010 |
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Enhancer Sequence | GCAAGACTCC GTCTCAAAAA AAAAAAAAAA AAAGAGTGTG GAAGTGCTTA ACACAGAAAG 60 ATAAAATGTG AACTTTCATT AGATTATTTG TCGACATTTG GTGGTAGATA AACCAACAGC 120 TCTTTCCAAC TCCCCTGAAA TTTTCCCACG GCTTAATTGA CAGGGGAATG GGATGTTTTG 180 GTTGGACATT TCTATACAGT CACTTAAAAA TCCTCTCCGA AGGTGTTTCT TCCCTTCAAA 240 ATCAGAGAAA AGACACATTT AGTGATGAGA ATCAAGAGCT AGACAGGGGA CACTTGGTGT 300 TTGGAATTCT TCACCAAATC ATTTCACTTC CTTTGTTTCC TCAGGGAGGA AGGCAACCAC 360 AGCCTCTGCA TTTGCTCCCT GACTTGGTTT ACAAGGTTAG TCAAATACCC TGTACCACAG 420 AGTGGCTGGG TTAATGATTT ATCTAAATGA GGTAAAAGCC ATATCTATTG CAACGCTGCG 480 TTTCAGTCTA TTTTCCCAAA CTGGTTAGCT ATTGCACACT AATGATGTAG CTTAATGCTG 540 TGTCACTAGG CTGTTCTAGA ACATTTGTGT ATATTATGTT CACAGTGCTG AAAGAAGCAA 600 CTTTCCTTTT TAATAGTTAC AGTCTTTCTG AAAGCCCTGG AAGAAAAAAA AAAGTGACCC 660 TAAGAAACAA GATAGCATTC AGGTAATGTT TAAATCAGAC TGTATCTCAG ATCAAAGGGC 720 ACTTCTTTTT TTTTTAATTG AGATAGAGTT TCCCTCTTGT TGCCCAGGCT GGAGTGCAAT 780 GGCACAATCT CAGCTCACTG CAACCTCTGT CTCGCAGGTT CAAGCAATTC TCCTGCCTCA 840 ACCTCCCGAG TAGCTGGGAT TACAGGCATG CGCCACCCCA CCTGGGTAAT TTTTTTTTGA 900 GATGGAGTCT CCCTCTTGTT GCTCAGGCTG GAGTGCAATA GTGCAATCTC GGCTCACCGC 960 AACCTCCGCC TCCCAGGTTC AAGCGGTTCT CCTGCCTCAG CCTCCAGAGT AGCTGGGATT 1020 ACAGGCATGC ACCACCCAGC CCGGCTAATT 1050
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