Tag | Content |
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EnhancerAtlas ID | HS091-19343 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:28545950-28548630 |
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) |
Gfi1b | MA0483.1 | chr17:28546803-28546814 | AGCTGTGATTT | - | 6.14 | Myod1 | MA0499.1 | chr17:28546490-28546503 | AGCAACAGCTGCA | - | 6.64 | Nr2f6(var.2) | MA0728.1 | chr17:28548213-28548228 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH17I030219 | chr17 | 28546062 | 28547978 |
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Enhancer Sequence | TGAGGCAGAT GAAAGACAAT TTCACTCCCT GCCCACGTCT GTCCCAGGAT AGCCCAACCA 60 ATCTGTGACT GAGAATCACA GTCGCCGGAT GATGTGAGTG TCAGGAGCCA CCCTGGGCTG 120 AGTGGCCTCA TGCTGTGCTC CTCTGGTCTC AGTGCTTTGC TAGAAGCAGT CGTAGGGGGA 180 GCACCATGAC TAAAATGAGG TTTCAGAGGA GGCCAAGAGA GCAATTGGGA AGAAAGCCTG 240 GTTTGGGAGT CGACAGAACA GGCAGGATCA CATCCACTTA TGACTACCTG GAGAACGCTG 300 GGCCACTTCC CCTCTCTGAG CCCCAATTTC CTCCCTATAA AAGAACACAG TTGAGGAGAG 360 CTGAGTTTCC CAAATGTAGC CACACATCAT AGTCACCTAG ATTCCTGGGT CTACCCCAGA 420 CCTCCTGAAG CGGAATCTCC AAGCATGGGC ACAACACAAA AATTGTGTTC AAGCTCCCTA 480 GGTGATTCCG ATGCAGCCAG TACCTGGGAC CCTTGGAACA GATCACCTGT GACAATCTGT 540 AGCAACAGCT GCAACTCTCT GTGAGTCACC AAATCAGTAT CTTTGTTCAT CAGTATTATC 600 TATGGCTCCA GACACATGAT TATTGATATT TGGCTACACT TCCATAATTC CATTGAGCCA 660 GAATGCTCCC TGACAAGCGC CGTTTGCAGG AGTGGCTGGA CAGGGTAGTT TTTCACAGAA 720 CAAGCAAGCA CAGAGCTGCT ACCTAACTGG AGATGCTGGT GTCTCCTGGA TCTTGTGGCT 780 GAGGCTGAAT TTAAAAATAC CAAGTTGGGG AATGCTAACC TGCAGCCTGA GTTTTTAGCC 840 TAAAGGGTGG ATCAGCTGTG ATTTTCCCTA ATTTTCCCTG CTGTAAAATG CTCTGAACCC 900 AGAAACCTGA GGTCTGTGCA AATCAGAAAG GTCCATGTAA TTTACAGTCA CACTGGGTAA 960 ACCCGGCTCG AGAATAAAAC CATGTGTTCT CGTGATGGCC TTCCTCCAAA GAGTTTGCTT 1020 GATCAGCTTT ACGCTGGGGA ATGAGTGTCG GGGAAATGTC ACCAGTGACC CAGCCCCTTA 1080 CATAATGCCC AGGCTAAAGG TGAGTCCTCT GGAGCAGGAG ATAAGGTGAT TATGACTTTT 1140 GCTCCTCCTA GGCAGGAAGC GCTGAGCTTC CCAGGGGCCC CCTGGAACTA CCTTTGCAAC 1200 TACATGGACA GAAATCTTTA AAAGAGAGTA AATCCAGGCC ACTCTGTGTT AGGTCACGGG 1260 AGAAGTGAGG GTGACACAAA TGGATGATCC CCAAACCTCT TTGTAGCTGC CCTCCCAAAT 1320 CTGTTGTCAG AGTTCCCATG AAAATCAAGC TTGACGCATC TGACACCCAC TTCTTGTTAT 1380 TTTCTTGTGC TGATAACAAG TCCAGAGGCC CCAAACCCAT TCACTTTTCC CCACTGCTCT 1440 GCTCTCCCCC AGGTTCCCAT CTTCATGCCT ACAGTCAGCT ACTATTTTTT ATAATCTACA 1500 AGTTAACTAC TTGAGAGGCT TTAGGGGTAC AAGGAACAAG ATAGGGCCTC TGGCCTCAAA 1560 AATCTAACAT CCCAGGAGGA GATAGGAGGG CCAGCCATGC GTGGTTTGAG GTTGGTATTA 1620 ATGTCATGCT GTGGATCTAA TCCAGCTTAA ATTCTGCCCA GACTGGTAAT TAAGATTTAG 1680 GACTTAACGC TGATGCCCTT CTCTGACCTC ACACAGGTCC AAAGGATCAG AAGCATCTGG 1740 GACTCTGAAG CCACCTCCAA ATTTTCCCTT ACGCAGGCCT ACCCTCGTGG ACTCTTCCCA 1800 GCAGAACTTG CCAGCAGGAG TGAAGGGACT CAGCACAGGG CTGACGGCCA TTCCCTCACT 1860 TCTGGCTGGG GGAGGACAGA GCCTGGAGAA TGCAGGATGA GAAGGAGGCC CTTCAATAAA 1920 TGGAGCGCTA ATGATGCTGG AGATCTGTGA GGTCAGGTTT GGGAGGGCTT CACCCAGCTT 1980 CACAACCCGG AGAGCCTCAG ACACGCTGTC TTCAGCTTTT GGCTTGCTGG AGATTTGACT 2040 TTTTTTTTTT TTTTTTTTTT TTGAGACAGA GTCTCGCTCT GTCGCCTAGG CTGGAGTGCA 2100 GTGGTGCCAT CTCGGCTCAC TGCAACCTCC ACCTCCCAGG TTCAAGTGAT TCTCCTGCCT 2160 CAGCCTCCCA AGTAGCTGGG ACTACAGGCG CCCACCACCA TACCCAGCTA ATTTTTATAT 2220 TTTTAGTGGA GACGGGGTTT TGCCATGTTG GTCAGGCTGG TCTTGAACTC CTGACCTCAG 2280 GTGATCCACC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACCACGCCT 2340 GGCGAGATTT GACTTTTCTA CCAGCTCGAA AGTCTAAGTC ATCATGTTCC TAGTCTTACG 2400 CCAGTGAAGA CTGAAAAGAC ATAATCTGTC TTCTGGCCTC TCAAGAGGAC CTACAGCCCA 2460 TCCCAGGTCA CAGCCCACCC GGGTCACAGC CCACCCCAGG TCACAGCCCA CCCGGGTCAC 2520 AGCCCACCCC AGGTCACAGC CCACCCGGGT CACAGCCCAT CCCAGGTCAC AGCCCACCCC 2580 AGGTCGCAGC CCACCCGGGT CACAGCCCAC CCCGGGTCAC AGCCCACTCC GGGTCACAGC 2640 CCACCCTGGG TCACAGCCTC TACTCGCAGC CTGTGATACT 2680
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