Tag | Content |
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EnhancerAtlas ID | HS091-15792 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr15:99507760-99509270 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr15:99508294-99508306 | ACAATGTAAACA | - | 6.04 | Nr2f6(var.2) | MA0728.1 | chr15:99508640-99508655 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 99508101 | 99508269 | chr15 | 99508857 | 99509004 |
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Enhancer Sequence | TTCTGTCTCT GGTTTGGTTT TGTCCCTCCT GGAAGCATCA CTACACTTTG GTGGCAGGGA 60 AGCTGAGCTA TGTGGGGCAC GTGTGTTCAC GCATGTTGCC TGGAAGCGTT CTCCAGAAAA 120 GCATTGCCTC TTCTCTGACA GCTGAGCTTT CTCAGCATGC AGATTGCCAG TAAAGACGAC 180 AGGGAAGCTA TCTGTTTCTC CCTCCATTAA ATCATCTGGA AAGAAATTTG AATACATAAA 240 TTACGAAACT CTGTACTGCA GTTCCGACTG ATTTGTAGAC TTTTTTCCTA TACCTTCCAC 300 TAACAACAGT CAGGCCAAGG CAAGTCTGAT CTGCATGACC CCAAGGCAGA GGACTTCAGT 360 TCTTCACATT TCCCATGTGC TTTTTGGTCT TTCACAGCTG ACATGCCCAC CTCGGGGGGA 420 TGCTGGTGAG AACCCAGTGG GCCTCACGCA GAATGTGGGT CACTGGAGGA GCTCCAAAGT 480 CCTAGTTACT TTCTAGCTGC TGCTCAGTGA TCTCTGTCTG CCCCTAGGGA CCCTACAATG 540 TAAACATTAT TTTTGTCAGG GGAAATGGCA TGTATGGCAA GGTGTGTTCT AGAATCAGAC 600 TAAGGATTCA GACACATCAG GCAGAGAAGC TGGTCATTTC CTTCAACTTT ATCATGGGAA 660 ATTATGCTCC AATAGCAAAA TCGGGCCAGT AGAAGAAGAG CTGTCCAGCA ATGTATAGGT 720 AGAAGTAAAC CGAAGACCAT GGTTACTTCA GACCTGTTGA GCCTCAGAAG TGTTTGCACC 780 TAAAAGCAAA GGCCTTTCTG AAAGGGGACT CTCAGCTGGG GTGCGGTGGC TCACGCATGT 840 AATCCCAGCA CTTTGGGAGG CTGAGGTGGG TGGATCACAT GAGGTCAGGA GTTCAAGACC 900 AGCCTGGCTA ACATGGTAAA ACCCCATCTC TACTAAAAAT ACAAAAAATT AGTGGGACAT 960 GGTGGCGGGT GCCTGTAATC CCAGCTACTT GGGAGGGTGA GGCAGGAGAA TCTCTTGAAC 1020 TCAGGAGGCA GAAGCTGCAG TGAGCCAAGA TTGTGCCACT GTACTGCAGC CTGGGTGACA 1080 GAGTAGGACT CTGTCTCAAA AAGGGTACTC AAGCTTGGCA TTGCTTCAGG GTTACTGCTC 1140 AGTGTTGTCA CCGAGTGCCT GGCACTCAGG GGATCTTCAT TAGGTGACTG ATGATGAGGA 1200 GGTCTCAATT CTGAGGCTGG AAAGCCCAAC AGGGCCTCCT CCTTCCCTGG TCAGGTAGAT 1260 GCTGCCCTTC CAGGTTGCCA CAGTGCAGTC TGCACTTGGC CTGCCCAGCC AGAAGGAGCA 1320 GCAATATCTA AGGATGAAGG TGCTGGGTCT TCAGAAGCAT TAGAACCTTT CCCCTCCAGG 1380 CCATTTCTTA AGACTGCAAG CCCTCAAGAG CTATTTCTGC ATTTACCCCC CAAGTCCAGG 1440 TATGAGTCCA TACTCACTCA GATGTGTGAT TTTTGTAGTG TTCTAATGTT GCTAAAAAGA 1500 CCTTCACATC 1510
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