Tag | Content |
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EnhancerAtlas ID | HS127-15097 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr19:13023290-13025830 |
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: 2 | Chromosome | Start | End |
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 | CCTACTCATT TGTTTTGCAG CACCCCAAAG GTTTCATCAG TTTGCTGAAT ATCTAAATGA 60 ATGCAGCACT GACATTGGGG CTCCCACACC TCCTCGTACC CAGTTCACCT TGTTGTCTCA 120 GCCTCTCCTG GATGCTCTCA ACAGTTTCAG ACCCTAAAAT TAAAATCGAT GAGAGCACCA 180 GGTGTTTCTT TTTGTGTGAT TGTTCACAAC CTGCTTGAGC TGCTAATGGT TCAGAGCTGC 240 TCCTTTTTAA GGCTCAAGGG ATGAGGCTGG AACCGGTTTT CATGGCAGCT AAGCAAACAG 300 TAAAAAAAAA AAAAAATCAC TTGAATTCAG CTAATTCGAG TTTCATGGTA GGACAAAGGC 360 CTGCATCAGA TGTCTGCTGA GAGCTTCTTT ATTTTTCCAA CCTCTCCTTT GGGGATTTAT 420 CCCTTTTGAT TTCATTTTTC TTAATACACA GCAGCTGCAT ATTAATCAGG ATGCTAATGA 480 ATCATAGGCT TCCCTGGGCC TGCATTCACC AATTAACTTT AACAAACAAA ATGCGTGGTG 540 TCCTCTCTGC TGGCTTTCCC GGTTCCTAGG CTGGCTTCTG TTGCCGAACC CTGGACCGAG 600 GCCAGAGAAT GCAAGTCAGC CCAACACAGC ACGTCGGGTG TGCATGGCCT GCGCCCGGAT 660 TGGGCAGCGG GCTGGGGGCT GTGAACACAG CGCTGCGTTC ATCTATTATG GTCTGTCCTT 720 CTAAGAAGTC CCTAATTTGG CTGCGAGGAT TAGGACATAG TTCCCAAGCA GGGCCCACGC 780 TGGCAGGGGG CCCAGGAGCT GCGGAGGAAA TGGGTCTAAG CGAAGAGACC ATCTGTTCGC 840 TCCAGGTAAA GCTGTGATTG GCAGGCGACT GAGCCAGAAC TGCCCGCTGG TGGGGCCCTC 900 CCTCCGTGGC CTCTAACAGA TATACAAGTA AACAATCCGC CAGCCACTTA TGACCACCGA 960 GGGTGGCAGT CCCGGGAGAG GAGGCAAGCT AATCAAACAT TCAAGGGGGG AACACAACAG 1020 AATCTCTGGC GCTTGGGCAA AACAATGTTT TGCTGAAGTA CAGCCAGGAA GGGGGAAGGT 1080 TTGAATGGAA GCTGATGAGC CAGTTCCTCA ACCTCTCCTT TTCTCTCTGG AAACGTGTTA 1140 ACATTTTAAT CATGTTGCTG AGTATCTGCT GCTGGATCTA TTAACTGGCC CCTGCACTGG 1200 TTTTAATCTA TCTGTTTTTT GGCCCAGGGT TCCTGTGGAG CTCCTTGAAG TCTCTAAATG 1260 ATTTGCAGCG GTCTGTGTCT CTTCACTACA CAGATCCTGG TCTAAACATG CTATTCCGCA 1320 GTAAGGTATT AGCAAACAAA CGACTTCAAC CATTGCTTCC CTTTTTTTTT GGTCTCCAAT 1380 TGACAGCACA CACCTATAAA CCATTTCACG CGTGGCCTGC TTTCCAGCAG AGGAATGTGC 1440 GAGGAGAGGG AAGCTGGCTT GCTTTCTGCC TAGAGTCCTC AGGGCCCTGT CCTGACCCTC 1500 CTCTCACTCC TTCTCCAGGT GAGCTCATTC ATTCCACAGC TGCTGCTGAA ACAATGACTC 1560 CCACAGAACC ATCTCCAGAC CCTCACCCCA CCCCGAGTTC CGGGTCAGAA AGTTGAACTG 1620 TATCCTGGAC ATGTGGATGT CCCTGGCCAC CGAAAGTGGC TCAGATAAAC AAGGACAACA 1680 CAGAACTCAT GTTCTTGTCT CTGCCAGAGA AGCCACCACC TACCGGAAAC CACCACAAGC 1740 TGGAAAGCAG ACAGCAGTGA TGTGCTTGTA AGCATTTAGC AACTGGCTGT GTGATGGGGG 1800 GGAAGCCCTG ATTCGTAGTG TTTGCCAATT TCCGTGGTGC AGAGCCTCCC ACCATTAGCC 1860 AATTTCAGGC TACCAACATG AAGACGCTAA ATGCCAAGTT GGGAAGAGAT GTGTAGAATT 1920 GGCTCTTTCA AGCCGGTAGG AGCTGGCCCC AGTACATCAT GGCCGGGAAA CATCCTCCCT 1980 CATCCCCTTC CTGTGTCTTA TGGCACAAGG CACTTCCTCC ATCTGCCCTG CTAAAGGCCA 2040 CCCCCCCCAC ACCCCCCATA AAAGCCTCCC ACTAGACCTC CCTACACCCA CACATTCTCC 2100 CTCCCAACCA TTCTCTACAA AGCAGCCATA TTTTTTTATT AATATTTTTT GAGACAGGGT 2160 TTTGTTCTTG TTGCCTAGGC TGGAGTGCAA TGGTGCAATC TTGGCTCAGT GCAACCTCTG 2220 CCTCCCAGGT TCAAGCGATT CTCCTGCCTA ACCCTCCCAA GTAGCTGGGA TTACAGGCAT 2280 GCACCACCAC CCCTGGCTAA TTTTGTATTT TTAGTAGAGA CGGGGTTTTG CCATGTTGGC 2340 CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCCATCTA CCTCGAACTC CCAAAGTGCT 2400 GGGATTACAG GCATGAGCCA TCGTGCCCGG CCTGCAGCCG TATCTTTTTA TAACGGGAAC 2460 CTGAGCATGT CACTTCTGTG ACCCAGCAGT TCCCCTCCTA GGTATGAGTA TGCCCAGAAG 2520 AAATGAAATC ATCTGTCCAC 2540
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