Tag | Content |
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EnhancerAtlas ID | HS118-13513 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr3:171076100-171077500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr3:171076762-171076777 | AGTTAATATTTAACT | + | 6.05 | HNF1A | MA0046.2 | chr3:171076762-171076777 | AGTTAATATTTAACT | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 171076448 | 171076930 | chr3 | 171076705 | 171076800 | chr3 | 171076800 | 171077043 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I171357 | chr3 | 171075364 | 171077425 |
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Enhancer Sequence | ACATGGCCGG GGAAGCCTCA CAGTCATGGC CGGAAGTGAA TGAGGAGCGA AGTCACATCT 60 TACATGGTGC AGACAAGAAT GCTTGTGTAG GGCAACTCCC CTTTATAAAA CCATCAGGTC 120 TCTTGAGAGT TATTCACTAC ACGAGAACAG TATGAGGGAA ACTGCCCCCA GGATTCAATC 180 ATCTACACCT GGCCCCACCC TTGACCGGGG ATTATTACAA TTCAAGGTGA GATTTGGGTA 240 GGGAGACAGC CAAACCATAT CAGAAAACAT ACACAATATT CTTTTAGGAT TCATACAAAA 300 TGCTTGCGTA TTTTTTGTGG ACTTCTACCT GAGAAGGATC GTTTTATTTA GATATAAACA 360 GGGTAGAAAA ATCAAGGGCT TCAGCTGGTT TCAGCTTCCT AGAACAAGAT GCAGCCCTGC 420 AGTTGTGGGG CGGTCAGTCA CCTGCAGATA ATAAAGTGGG CTGTTGGTGA GGTACCTTGG 480 AGGAACGCCA ACGTAAGGAC AGACAGACAT GCAGACCCAT TTCAAGCTTG TTGCAGATCC 540 AGTGTTGCAG GACATGACCC AGGAAACCAC CACCTCTATA ATTAAGTTTT AAGTTTACTA 600 ACAGTATTTT TTTAAACAGA GATCAGGGCA TGGGGTGGAG TGAGGGATAG TAGGGTATGG 660 GGAGTTAATA TTTAACTGGT TCAGGGTTTC AGTTGAGGAT GATGAAAAAG TTCTGGAGAT 720 GGGTAGTGGT GAAGGTTGCA CAACAATGTG AATGTACTTA ATGCTGCTGA ATTGTATGCT 780 CACTTAAAAT GGCTAAGGGG GTAATTACTG TATGTACGTT CTACGATAAG AGAAAGAGGT 840 ACCACTAAAA AGATTTCCAG TAAGATAAAT TCAGCTAGGA GCCTCATACC ACCTCCCTGA 900 ATGTGATGCA CAGATCAAAA CTGAATTTCT CAAGCCATAC TCGAAGTATC AACTCGAAGA 960 TGTTAAACAG TAACGGGCAA GTTTTCTAAA ACAAGAAGTC ACCTTCTCCT TAAAGGAGAC 1020 TGAGTTCTTC ACATATGGAG TTCCTAACTC TTCCCTGCTG TCCACAAAGA TGATATGGTT 1080 ATTATTATCA TGATTGTTGT AACAGACATT TTGTAATTTA TCTAGAAAAA TTGTGTAACC 1140 AGCTGCTACA CTTGTCTGCC TTTGTTGTAG AGAGGAACAA AATGGACACA GTAGTTCTGT 1200 GCTTCTCCTT GCAAAGTGAG CAACAGGACC AAGATCCGAA GCAATATCAG AGGCCACTGC 1260 ACCCAGCAGC AGAGGTTGTA ATGACCCCAT TCTAGACCCT CACCACCAAC AACGCTCCTA 1320 TGTAGTAGTA AGCATATATT TGCTTGCCGA ACAGCAGATA TTTCTTTTTG CATATGCAAA 1380 ATATCCAAGC AGATTTAATG 1400
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