Tag | Content |
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EnhancerAtlas ID | HS060-17207 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:13023170-13025730 |
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) |
ESX1 | MA0644.1 | chr19:13023797-13023807 | ACCAATTAAC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr19:13025641-13025656 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr19:13025331-13025351 | CCCCCCCACACCCCCCATAA | + | 6 | ZNF263 | MA0528.1 | chr19:13024785-13024806 | CCCTCCTCTCACTCCTTCTCC | - | 7.48 | ZNF740 | MA0753.2 | chr19:13025327-13025340 | CCACCCCCCCCAC | + | 7.52 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 13023244 | 13025372 | chr19 | 13023589 | 13024232 | chr19 | 13024661 | 13024953 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I012911 | chr19 | 13022750 | 13026005 |
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Enhancer Sequence | ATTTGGAACT TTTGCTTCTC TACCCCCCGC TATACCTAGG CCTTGCTGGT CACAAAGCTG 60 CCAAAGTTTA TGAACATCAG TCCCCTCCAG CGCACGACAC CTTGAGGGTG CAGACTACAC 120 CCTACTCATT TGTTTTGCAG CACCCCAAAG GTTTCATCAG TTTGCTGAAT ATCTAAATGA 180 ATGCAGCACT GACATTGGGG CTCCCACACC TCCTCGTACC CAGTTCACCT TGTTGTCTCA 240 GCCTCTCCTG GATGCTCTCA ACAGTTTCAG ACCCTAAAAT TAAAATCGAT GAGAGCACCA 300 GGTGTTTCTT TTTGTGTGAT TGTTCACAAC CTGCTTGAGC TGCTAATGGT TCAGAGCTGC 360 TCCTTTTTAA GGCTCAAGGG ATGAGGCTGG AACCGGTTTT CATGGCAGCT AAGCAAACAG 420 TAAAAAAAAA AAAAAATCAC TTGAATTCAG CTAATTCGAG TTTCATGGTA GGACAAAGGC 480 CTGCATCAGA TGTCTGCTGA GAGCTTCTTT ATTTTTCCAA CCTCTCCTTT GGGGATTTAT 540 CCCTTTTGAT TTCATTTTTC TTAATACACA GCAGCTGCAT ATTAATCAGG ATGCTAATGA 600 ATCATAGGCT TCCCTGGGCC TGCATTCACC AATTAACTTT AACAAACAAA ATGCGTGGTG 660 TCCTCTCTGC TGGCTTTCCC GGTTCCTAGG CTGGCTTCTG TTGCCGAACC CTGGACCGAG 720 GCCAGAGAAT GCAAGTCAGC CCAACACAGC ACGTCGGGTG TGCATGGCCT GCGCCCGGAT 780 TGGGCAGCGG GCTGGGGGCT GTGAACACAG CGCTGCGTTC ATCTATTATG GTCTGTCCTT 840 CTAAGAAGTC CCTAATTTGG CTGCGAGGAT TAGGACATAG TTCCCAAGCA GGGCCCACGC 900 TGGCAGGGGG CCCAGGAGCT GCGGAGGAAA TGGGTCTAAG CGAAGAGACC ATCTGTTCGC 960 TCCAGGTAAA GCTGTGATTG GCAGGCGACT GAGCCAGAAC TGCCCGCTGG TGGGGCCCTC 1020 CCTCCGTGGC CTCTAACAGA TATACAAGTA AACAATCCGC CAGCCACTTA TGACCACCGA 1080 GGGTGGCAGT CCCGGGAGAG GAGGCAAGCT AATCAAACAT TCAAGGGGGG AACACAACAG 1140 AATCTCTGGC GCTTGGGCAA AACAATGTTT TGCTGAAGTA CAGCCAGGAA GGGGGAAGGT 1200 TTGAATGGAA GCTGATGAGC CAGTTCCTCA ACCTCTCCTT TTCTCTCTGG AAACGTGTTA 1260 ACATTTTAAT CATGTTGCTG AGTATCTGCT GCTGGATCTA TTAACTGGCC CCTGCACTGG 1320 TTTTAATCTA TCTGTTTTTT GGCCCAGGGT TCCTGTGGAG CTCCTTGAAG TCTCTAAATG 1380 ATTTGCAGCG GTCTGTGTCT CTTCACTACA CAGATCCTGG TCTAAACATG CTATTCCGCA 1440 GTAAGGTATT AGCAAACAAA CGACTTCAAC CATTGCTTCC CTTTTTTTTT GGTCTCCAAT 1500 TGACAGCACA CACCTATAAA CCATTTCACG CGTGGCCTGC TTTCCAGCAG AGGAATGTGC 1560 GAGGAGAGGG AAGCTGGCTT GCTTTCTGCC TAGAGTCCTC AGGGCCCTGT CCTGACCCTC 1620 CTCTCACTCC TTCTCCAGGT GAGCTCATTC ATTCCACAGC TGCTGCTGAA ACAATGACTC 1680 CCACAGAACC ATCTCCAGAC CCTCACCCCA CCCCGAGTTC CGGGTCAGAA AGTTGAACTG 1740 TATCCTGGAC ATGTGGATGT CCCTGGCCAC CGAAAGTGGC TCAGATAAAC AAGGACAACA 1800 CAGAACTCAT GTTCTTGTCT CTGCCAGAGA AGCCACCACC TACCGGAAAC CACCACAAGC 1860 TGGAAAGCAG ACAGCAGTGA TGTGCTTGTA AGCATTTAGC AACTGGCTGT GTGATGGGGG 1920 GGAAGCCCTG ATTCGTAGTG TTTGCCAATT TCCGTGGTGC AGAGCCTCCC ACCATTAGCC 1980 AATTTCAGGC TACCAACATG AAGACGCTAA ATGCCAAGTT GGGAAGAGAT GTGTAGAATT 2040 GGCTCTTTCA AGCCGGTAGG AGCTGGCCCC AGTACATCAT GGCCGGGAAA CATCCTCCCT 2100 CATCCCCTTC CTGTGTCTTA TGGCACAAGG CACTTCCTCC ATCTGCCCTG CTAAAGGCCA 2160 CCCCCCCCAC ACCCCCCATA AAAGCCTCCC ACTAGACCTC CCTACACCCA CACATTCTCC 2220 CTCCCAACCA TTCTCTACAA AGCAGCCATA TTTTTTTATT AATATTTTTT GAGACAGGGT 2280 TTTGTTCTTG TTGCCTAGGC TGGAGTGCAA TGGTGCAATC TTGGCTCAGT GCAACCTCTG 2340 CCTCCCAGGT TCAAGCGATT CTCCTGCCTA ACCCTCCCAA GTAGCTGGGA TTACAGGCAT 2400 GCACCACCAC CCCTGGCTAA TTTTGTATTT TTAGTAGAGA CGGGGTTTTG CCATGTTGGC 2460 CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCCATCTA CCTCGAACTC CCAAAGTGCT 2520 GGGATTACAG GCATGAGCCA TCGTGCCCGG CCTGCAGCCG 2560
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