Tag | Content |
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EnhancerAtlas ID | HS189-01409 |
Organism | Homo sapiens |
Tissue/cell | Thymus |
Coordinate | chr19:13023750-13025890 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I012911 | chr19 | 13022750 | 13026005 |
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Enhancer Sequence | ATTAATCAGG ATGCTAATGA ATCATAGGCT TCCCTGGGCC TGCATTCACC AATTAACTTT 60 AACAAACAAA ATGCGTGGTG TCCTCTCTGC TGGCTTTCCC GGTTCCTAGG CTGGCTTCTG 120 TTGCCGAACC CTGGACCGAG GCCAGAGAAT GCAAGTCAGC CCAACACAGC ACGTCGGGTG 180 TGCATGGCCT GCGCCCGGAT TGGGCAGCGG GCTGGGGGCT GTGAACACAG CGCTGCGTTC 240 ATCTATTATG GTCTGTCCTT CTAAGAAGTC CCTAATTTGG CTGCGAGGAT TAGGACATAG 300 TTCCCAAGCA GGGCCCACGC TGGCAGGGGG CCCAGGAGCT GCGGAGGAAA TGGGTCTAAG 360 CGAAGAGACC ATCTGTTCGC TCCAGGTAAA GCTGTGATTG GCAGGCGACT GAGCCAGAAC 420 TGCCCGCTGG TGGGGCCCTC CCTCCGTGGC CTCTAACAGA TATACAAGTA AACAATCCGC 480 CAGCCACTTA TGACCACCGA GGGTGGCAGT CCCGGGAGAG GAGGCAAGCT AATCAAACAT 540 TCAAGGGGGG AACACAACAG AATCTCTGGC GCTTGGGCAA AACAATGTTT TGCTGAAGTA 600 CAGCCAGGAA GGGGGAAGGT TTGAATGGAA GCTGATGAGC CAGTTCCTCA ACCTCTCCTT 660 TTCTCTCTGG AAACGTGTTA ACATTTTAAT CATGTTGCTG AGTATCTGCT GCTGGATCTA 720 TTAACTGGCC CCTGCACTGG TTTTAATCTA TCTGTTTTTT GGCCCAGGGT TCCTGTGGAG 780 CTCCTTGAAG TCTCTAAATG ATTTGCAGCG GTCTGTGTCT CTTCACTACA CAGATCCTGG 840 TCTAAACATG CTATTCCGCA GTAAGGTATT AGCAAACAAA CGACTTCAAC CATTGCTTCC 900 CTTTTTTTTT GGTCTCCAAT TGACAGCACA CACCTATAAA CCATTTCACG CGTGGCCTGC 960 TTTCCAGCAG AGGAATGTGC GAGGAGAGGG AAGCTGGCTT GCTTTCTGCC TAGAGTCCTC 1020 AGGGCCCTGT CCTGACCCTC CTCTCACTCC TTCTCCAGGT GAGCTCATTC ATTCCACAGC 1080 TGCTGCTGAA ACAATGACTC CCACAGAACC ATCTCCAGAC CCTCACCCCA CCCCGAGTTC 1140 CGGGTCAGAA AGTTGAACTG TATCCTGGAC ATGTGGATGT CCCTGGCCAC CGAAAGTGGC 1200 TCAGATAAAC AAGGACAACA CAGAACTCAT GTTCTTGTCT CTGCCAGAGA AGCCACCACC 1260 TACCGGAAAC CACCACAAGC TGGAAAGCAG ACAGCAGTGA TGTGCTTGTA AGCATTTAGC 1320 AACTGGCTGT GTGATGGGGG GGAAGCCCTG ATTCGTAGTG TTTGCCAATT TCCGTGGTGC 1380 AGAGCCTCCC ACCATTAGCC AATTTCAGGC TACCAACATG AAGACGCTAA ATGCCAAGTT 1440 GGGAAGAGAT GTGTAGAATT GGCTCTTTCA AGCCGGTAGG AGCTGGCCCC AGTACATCAT 1500 GGCCGGGAAA CATCCTCCCT CATCCCCTTC CTGTGTCTTA TGGCACAAGG CACTTCCTCC 1560 ATCTGCCCTG CTAAAGGCCA CCCCCCCCAC ACCCCCCATA AAAGCCTCCC ACTAGACCTC 1620 CCTACACCCA CACATTCTCC CTCCCAACCA TTCTCTACAA AGCAGCCATA TTTTTTTATT 1680 AATATTTTTT GAGACAGGGT TTTGTTCTTG TTGCCTAGGC TGGAGTGCAA TGGTGCAATC 1740 TTGGCTCAGT GCAACCTCTG CCTCCCAGGT TCAAGCGATT CTCCTGCCTA ACCCTCCCAA 1800 GTAGCTGGGA TTACAGGCAT GCACCACCAC CCCTGGCTAA TTTTGTATTT TTAGTAGAGA 1860 CGGGGTTTTG CCATGTTGGC CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCCATCTA 1920 CCTCGAACTC CCAAAGTGCT GGGATTACAG GCATGAGCCA TCGTGCCCGG CCTGCAGCCG 1980 TATCTTTTTA TAACGGGAAC CTGAGCATGT CACTTCTGTG ACCCAGCAGT TCCCCTCCTA 2040 GGTATGAGTA TGCCCAGAAG AAATGAAATC ATCTGTCCAC ACACAAACTT TTCTAAATGG 2100 ATTTCATAGC AGTGCTGCTC ATAATAGCCA AAAAGTGAAA 2140
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