Tag | Content |
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EnhancerAtlas ID | HS091-11969 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr13:73559050-73560850 |
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) |
NFIL3 | MA0025.1 | chr13:73559058-73559069 | TTATGTAACAT | + | 6.32 | NFYA | MA0060.3 | chr13:73560516-73560527 | AACCAATCAGA | + | 6.62 |
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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 |
GH13I072985 | chr13 | 73559549 | 73560666 |
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Enhancer Sequence | CACATCTATT ATGTAACATA TAGACCTAGC AATTTTTAGG TTTCTTTTTT TAAGAATGAA 60 ATGTGTATTT TCCCACTGCA TTTTAGAAGC TTGTGATATG TTTTCGGTTA AATTAAAAGT 120 ACATTTCTCT GACCTTTTTT TGTCAGTAAG GAGCAAGTAA ATGACTTCTC TTGCTATCAT 180 TTCTAACCCT GTGCTTATAT GACTATCTTA GAATAGTAGC AGCTTATAAC AAACCAAACA 240 ATTCTGAGAC ATAAGGAGAC ACACACACAA AAAAAAACTA CAAAACTGTA AAATCTCTGA 300 AACTGTATAA TCTCTGAAAA TATTTGGTGG CCAGGCCGGG CGCAGTGGCT CACGCCTGTA 360 ATCCCAACAC TTCGGGAGGC CGAAGCAGGG GGATCACGAG GTCAGGAGAT CAAGACCATC 420 CTGGCTAACA CGGTGAAACC CTGTCTCTAC TAAAAATACA AAAAAAAAAA AAAAAAAAAA 480 AGCCAGGGCG GTGGCGGGTG CCTTGTAGTC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA 540 TGGCTGAACC CGGGAGGCAG AGCTTGCAGT GCAGTGAGCC AAGATCACAC TACTGCACTC 600 CAGCGTGGGC AACAGGGTGA GACTCCGTCT CAAAAAACAG AAAAAGAAAA AGAAAATATT 660 TGGTGGCCAG GAGACAATAT TAACAATTAT ATGAGATAAT TATAGTCATA ATTCTGTTAG 720 ACACCATATT GGCAATATCT TGTTGTAAAC TTAAGTCACT GATCCCGTAT CAAGGAGCTG 780 ACACTAAGAG AAGGCTGGAA TACAACATGG AGAAGGTACA GGCACTGGAG TGAGTCATAC 840 TCTGAAAACC AGTGCTCTAA GTGGAGGATA GGGTTTAAAG TCTGAAGTTG ATGCTGAAAA 900 TCAACAAGAA TATGCAACAA AACCCATCAA ACACTACTGA AATAGTAAAG GCCAGGGTCC 960 AGCACAGTGG GTCACACCTA TAATCCCAGG ACTTTGGGAG GCTGAGGCAG AAGGATTGCT 1020 TGGAGCCCAG GAGTTGTGTA CTAGCCTGGT CAACATAATG AGACTCCATC TCTAGAAAAA 1080 AAAATTTTTT AAAATAAATA ATTAGCTAGA TGTGGTGGCT CGTGCCTATA GTCCCAGCTT 1140 CATGGGAGGC TGAGGTGGGA GGACCACTTG ACCCCGGGAC TTCAAGGCTG TAGTGAGCTG 1200 TGCTTGCACC ACTGCACTCC AGCCTGGGCA AGAGTGAGAC CCTATCTCAA AAACAAAACA 1260 AAAAAGAAGG AAAAAAAAAT TTTGATGAAA AAGTTAAGAC CAGAAACTAG ACAGCAGCCA 1320 GATGACTACT GTTAATAGAA GGGAAAGCAA TTGCACTTGG TCACAAAGCC AGGCATCAAG 1380 AAAACATGAA TGTCAGAAAG CAGAGTGGGG AAAGTAGTGA GAAGTCCAGG GTAATCAGTA 1440 ATGAGATGCA CAAAAGGGTC TGAGCAAACC AATCAGAATA GAATTAAGGT TCCCACACTC 1500 CTGTTTTAAG TCAACAATAG CAGTAGATTT TAATTCAGGA ACCTACTTCA GTGTGTTAAT 1560 AATAGCTTCT TATCTGGATC ACTGTTGAGA ATTACCCTAA GATCATATCC ATGATTGTGA 1620 AAGAATGTTT CAGGTGATTA GTTATGTCCC GGAGGCTGTA ACAGCCCAAT TGTCTCTCAT 1680 TTGCTATCAT TCGTATAAAA GCATGAGCTC TCACTAAGCC TTCAGTCATA GATAGGGTAT 1740 AGCTCCAAAA ATGTTTCTGT CATCTTTTTT TTTTTTTTTT TTTTTTTTTG AGACAGAGTC 1800
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