Tag | Content |
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EnhancerAtlas ID | HS118-08480 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr18:847950-849290 |
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) |
STAT3 | MA0144.2 | chr18:848257-848268 | CTTCTGGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr18:848257-848271 | CTTCTGGGAAAAGG | + | 6.02 |
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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 |
GH18I000847 | chr18 | 847562 | 849415 |
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Enhancer Sequence | CCAGGCTGGT CTCGAACTCC TGAACTCAGG TGATCCACCC CGCCTTGGCC TCCCAAAGTG 60 CTGGAATTAC AGGTGTGAGC CACCACGCCT GGCGGCATTA CTAAATAATT CTAATAAACT 120 CACTAATACA CAATGTACTG AAAACCCAGG GGCTTTGAGG CCATCAGGAA TCCTTTAATG 180 GCCAGAGGGA CTGCTAGGGT CAGGCCCTTC TACCTCATTT CCACCACAGC TCACAGATGA 240 GGGCCTTCTA CTTCCTCTCC ACTCTGGCCA GTGTTGGAGG AAGCAGGTAC AGCCCCTCTC 300 TCTCTTTCTT CTGGGAAAAG GAGTGATTAG TTTGATTGTG AGCCTAGAAT ATTCACAGAG 360 GCAGGTTTTA CTCATCAGTG AGATTACTGT GCCCAAGACT TCACCCTTCC TCCTTCACTT 420 CCCACTTTTG CAGCAGCTTG GTCTGCATTC CTGCCCCAGC CACAGGCTAA ATGGCCAAAG 480 TCCTCTCGGA GCTGGGGCCT GGGCCAGTGG AAGGTGTGTG ACTCCCTCGT GCTATGTTGC 540 CCTTTGCTCT GGCAGTAGGA ATGCACTGTG CATTGGGATT TCCTTAGGCG GCAATAGTTC 600 CATCTACCCT AAGATTTGCA GGTGAAATGG CAGATATTTA TGGAGAAAGC AGTGGAAAGC 660 TCCACTACCC TCAGTCCTAA GCCTTTCTCC AGCCCAGCTT TTAGCAGAGT TTATGTCAAG 720 TGCTTGCTCA GCTTTTCACA AACAGCCACT GTCTTACCTC CTGAGGTCTT CCTGCTGTGC 780 AAGCTCCACC CGTTGGGCTG ACGAAAGGCG CTGGGAGCTC TGGGGCGCAG GAGCTGCCAT 840 CTTTGAAGCG CTCACACTGT GCTGGGCACT TTCTGTACCT TATCTTCTTT ATTCTTCAAA 900 ATGACTCTGG GGGATAGGTG CGGTCCCTGG TTCAAAGACG TGGAAGCAGA AAATTTGGGA 960 CATTAGTAAC TCTGGGCTAC TTAGTGAGTA ATAAAGCTGA AATTCAGTTT GTCTGGACTC 1020 TAAAACCTAT ACTTTTAGCA CTTTGAAGAC AAATTTGTTT CTTCCATGTT TTATGATATG 1080 GATTTATCAA CAAAGCCCTT CTCTTTGAGT TTCTGAGCGG ATCCAAAGCT GTTTTTTGAG 1140 AGAAATAATT GGTTCTGGCG GCACCCCTGA GGAAGCAGGA CAGGCTTGTC TCTGGCAAGA 1200 AAATAAATCA CGTTCCTCCA TTTTCCCAGC ACTTGCAGTC CTGCCATCTG CATGTCTGGG 1260 GCCTAAGACA TGTGTGTTTT CTTCTACTCA CAACACAGAA GACTGGCATT TACTCACTCA 1320 CCACTGAGTT GGTTGCAACT 1340
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