Tag | Content |
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EnhancerAtlas ID | HS118-07788 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr17:8963660-8966180 |
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) |
NR2F1 | MA0017.2 | chr17:8963829-8963842 | CAGAGGTCAACTG | + | 6.15 | Nr2f6(var.2) | MA0728.1 | chr17:8965240-8965255 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr17:8964509-8964530 | GGTGGAGGAGGAAGGGGAGGG | + | 8.54 |
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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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Enhancer Sequence | CAGTATCTAA TACATAAAAC ATATACAATA TGTATTATTA ACTGTTTATG TTATCCATAA 60 GGCTTCCAGT CAACAGTAGG CTACTATCAG TTCAGTTTTT GAGGAGTTAA AAGTTATACG 120 CGGGTTTTTT ACTGTGTGGG GCATTGGTGT CCCTAACTCC TGTGTTGTTC AGAGGTCAAC 180 TGTGAATTTT ATAACAGAAG ATAACCAGCA GTTGAGGACG GCCATGGTAA CTGTCAAATG 240 AATGGTTTTA ACATTGGGCT TCAGGAGGTG TGTAGCAAAC AGCACGGGGA CTCATAATAT 300 CTGTTTTGCC ATTAGCCAGC TAGCTCTCAA GTGGGATAAA AAGGAGTAGG CAGCCCGGGT 360 GCAGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGGCC AAGGCAGGCA GATCACGAGG 420 TTAAGAGATC GAGACCATCC TGGCCAACAT GGTGAAACGC CATCTCTACT AAAAATACAA 480 AAATTAACTG GGCATGGTGG CGCGTGCCTG TAGTCCAAGC TACTCGGGAG GCTGAGGCAG 540 GAGAATCACT TGAACCTGGG AGGCGGAGGT TGCAGTGAGC CGAGATTGTA CCATTGCATT 600 CCAGCCTGGT GACAGAGCAA GACTCTGTCT CAAAAAAAAA AAAAAAAAGT AGGCAACAAA 660 GGTTTAGGAT GAAGGTATAA TTTAAAAAGC ATGAAGTTGA AAAAATTACT CAACCACAGT 720 GACCTTGGTT GAATCACCTT AGGTTGTTTG CTTTGCACAG GGGAAAGATC ATCATGTTCT 780 TTTGTAGTGA TAGAGCATTC TGATCCAACC AACAGAGCCC CATGGTTTCT AGGGAGGTGG 840 AGAAGGCCTG GTGGAGGAGG AAGGGGAGGG CTCAGTTCCT TTCTAGAACT TGAGTGTCAG 900 TTGAAAATAG AGTGAGGAAG GTGGCAGTTG AAAATAGAGT GAGGAAGGTG GCTGATTCTA 960 GGCAGGTGAG TGGAATGAGT GACAGTGGCC CAAAGGGTAA GGGGGGGTCT GGCCTTTCTA 1020 GAGAACATGT GTCAATGAGA CAGTTGGCTG GAACCTTGGC TCCCAGTAGG AGCATAGGAG 1080 GAGATGGAGC AGAGACCGGG TATGGGCAAG GTGGTGGCCA GGCTAAGGAA GGTGGGGTTT 1140 ATCTAGACAA GTGGTTGTCA CATTTTGGCC TGCTTCAGAG TCACAGATTG CTGGGCCCTT 1200 CCTCAAAGAT AGGTTTGGAG TGGGGCCCTA GGATTTGATA TCTAACAAGT GCCCAGGTGG 1260 TGTTGATATT GCTAGTCTGT CCACATTTGG AGAACCACTG GTAAGCGATG GGCATCCAGG 1320 AGCAGTTTTT TTGTTGTTGT TGTTGTTTTT GTTTTATTTT GTTTTGTTTT GTTTTTTTGA 1380 GACGGATTCT CGCTCTGTCG CCCAGACCAG AGTCCAGTGG CGTGGTCTTG GCTCACTGAA 1440 ACCTCCACCT CCCGGGTTCA AGCAATTCTC CTGCCTCAGC CTCCCAAGTG GCTGGGATTA 1500 CAGGTGCCTG CCACCACGCT GAGCTAATTT TTTGTATTTT TAGTAAAGAC GGTGTTTCAC 1560 CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACCTCGTGAT GCGCCTGCCT CGGTCTCCCA 1620 AAGTGCTGGG ATTACAGGTG TGAGCCACCA CAGCCAGCCA GGAGCAGTTT TTAGCAGGGG 1680 ACAAGCCTGA TGAAATGGCG TAAACGATGG CCACTGGATA TGGCTGTGAG AGCAATCACT 1740 CATTAAATCA GGTGGTTTTG TTCCTGAATC AATCTTGCAT CTCAGTAGAT TTTTAGTCCC 1800 CGAGGCTCAG ACTGCCAACA AAAAATCTTT CAGGGCATTG TAATATTTTG ATGACCACAG 1860 ACTTCCTTGG AATGAAGTTG TCCCAATTCC GAATGAGGGG CCACGGCCTC ATAAAAGGTT 1920 TTTATTCCCC TTTCTGGGCT GGAGAAGCCA TCTAGGAAAA TGCTGTTTCT GTACCTAAAG 1980 TGTTGGGATT TTCAGATTGT TTTCATGAGT TACAGACACA CGGAGCAGCA TGCTTGAACT 2040 TAGACCCTTT CTGCAAATGT CAGGCTGTAT GATAATTGAG CCAGAATGTT ACTCGAGCTT 2100 TCTGACACAT TTTTTGAGAC CTCCCATCCA GTATTCTCAT ACAGAAATAT GGCTCCTCCA 2160 GGTGTGCACT TAACACTCGC TTCTTTGCAG CCAGGGGAAC CTTTAGCTAA GGAAAAAAAA 2220 GCCCTCCTAC CCTTGGTTTC AAAAGGTTTT GAAATGCTAA TTCACAACCA TGAAGTATTC 2280 TGACAGCCTG GAATGTTATT CAGGGCAATC AGGCACCTTG ATTATTACAG AAGTGTGAAA 2340 GGTAAATTGC TGCTACCCAA GAAGTCACCC AGCTTTTCAA GAGAAAGCTC AGAAAAATAG 2400 CACATAAAAT TATGTTCGGG GATTACACTT CATGTATCGT GTGATGGGGT GCTCTGACAC 2460 CCAGCGTGTC TGTAGGTGTC ACAACGTCAG CTCGTAGTAG AAATGTAACA GCATTTGCCA 2520
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