Tag | Content |
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EnhancerAtlas ID | HS091-47863 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:90094400-90095650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RAX | MA0718.1 | chr9:90095491-90095501 | GCCAATTAAC | + | 6.02 | SPIB | MA0081.2 | chr9:90094902-90094914 | CACTTCCCCTTT | - | 6.07 | USF1 | MA0093.2 | chr9:90094852-90094863 | GCCACGTGACC | + | 6.62 | USF2 | MA0526.2 | chr9:90094850-90094866 | TGGCCACGTGACCATT | - | 6.76 | ZNF263 | MA0528.1 | chr9:90094742-90094763 | TCTCTCTCTCCCCTCTCCCCC | - | 6.65 |
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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 |
GH09I087479 | chr9 | 90094481 | 90095548 |
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Enhancer Sequence | GTAGCTGGGA CTACAGGTGC CCGCCACCAC GCCTGGCTAA TTTTTTGTAT TTTTAGTAGA 60 GACGGGGTTT CACCGTGTTA GCCAGGATGG TCTCGATCTC CTGACCTCAT GATCCACCCG 120 CTTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA CTGCGCCCAG CCGGTTTTGT 180 ATTTTTAGTG GAGACGGGGT TTCACCCTAT TGGCCAGGCT GGTCTCAAAC TCCTGACCTC 240 AAGTAATCCA CCCACCTCGG CCTCCTAAAG TCCTGGGATT ATAGGCATGA GCCACCGCTC 300 CGGGCTGAGA TTCTTACAGC ATAGCTGATA TCAGAGTGCA TCTCTCTCTC TCCCCTCTCC 360 CCCAGGACTC TGGAGCCATG AGTAACACCA GGCAGGAGAG CACCCAGGAG TGTGTGGTTT 420 CTGTGGTGGC TGGGCCACTG CAAGTTTCCT TGGCCACGTG ACCATTCTTA GCCCAGGAAG 480 ACGACTCCAG TAGTACTTTC TTCACTTCCC CTTTCACTTC TCTTGTTCAC CAATGTTAAG 540 GGACCACCAG TTTTTAGAGA TTCACCCACA TTGTGAAGGT GGTGAGGTCA TGTTGCCACT 600 TTGACAATGA CATGGCATTT AATTTTTAAC CAAACCAAAT ACAGCATTCT GTCACTCGGG 660 ACAACCTTTG GAGACAGCTC CAAGGAAGTC TCCCCTCATG TTCTGCCTGC CGGATTAAAC 720 AGGAGTCTTG TTGAAGAAAA CATGAAACAG GGAAAGTTAA GACCTCAGCA GTCATAACTG 780 TTAATAAAAC ATGAGACTGC AAGAGGTGAT GTTAGAAAAG AAACTTAATG TCCGCCTAGG 840 TAATCATATC TTCTTATCGT GGGACCAAAG CATAAATGTA ACTCATATAT GTTTGTCCAT 900 TAAAATTAAG TGGTGGATCA CATCCCCATC CCTGTAAATA CTGGTTTGGA CACCTCCAGG 960 GGAAGGCAGG ACAATGGGAA ATTATATACA TAAAGGCAAA GGGACCAATT GAAAACTTCC 1020 ATTGCTAGAT CCTCACATGA CCTCTTTGAG GTCACATCCT ATTTATAATA GGCAAAGCAT 1080 AACCCTTCAG TGCCAATTAA CAAATGCTTT ATTAGGGTAT TTGCGTGTTT ATAACCATTG 1140 AATAATGTCC TTGCAAAGCG GCATCTTGCT GTCTATTTTC AGGTACTTAA TTAATGGCCT 1200 TGCTCCAGGA TAAACACATC CTGTGTTAAA TAAGACGATG AAAGCTTATA 1250
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