Tag | Content |
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EnhancerAtlas ID | HS187-11852 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:6862540-6863910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:6863757-6863776 | TAGTGCCCTCTGGTGGCCT | - | 8.06 | HINFP | MA0131.2 | chr19:6863018-6863030 | CAACGTCCGCAG | + | 6.27 | RREB1 | MA0073.1 | chr19:6863202-6863222 | GTGGGGGGGGCGGGTGGGGG | - | 6.26 | SPIB | MA0081.2 | chr19:6863667-6863679 | CACTTCCGCATT | - | 7.22 | ZNF740 | MA0753.2 | chr19:6863202-6863215 | GTGGGGGGGGCGG | - | 7.82 |
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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 |
GH19I006861 | chr19 | 6861602 | 6864330 |
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Enhancer Sequence | TGGAGAGGGA GGAAAGTGGG GGTGGGGTGG GTGAAAAGTT GTTGGGAGAC CGGGCGTGGT 60 GGCTCATGCC TATAATCCTA GCACTTTGGG AGGCCGAGGC AGGTGGATCA CTTGAGCTCA 120 GGAGTTCGAA ACCAGCCTGG CCAACATGGT GAATGTACAA CGGACAGCCC CCAATACAGA 180 CAGACAGACA CACACACACA CACACACACA CACTCACTCA CTCCTACCCC CAGCCCTAAG 240 AATTTACAAA CACTGATAAA GACAAATGAA ATCAGCGGAT ATAGACTTCA AACGCCGTCA 300 GACAGACACC CACTAGATCA AACAGGGACA TTCCTAAACA TCACACAGAC ACATCGCCAG 360 GCAGTCCCAC CGCAGACAGC CACAAATTAA AGCCGCGCTT GCCCCCTGAT GGACAGCAGC 420 AGTAGTGCGC CACCTCGATA GCGCAATCTC CCAGAGCGCT GGCATTGCAG GCGTGAGCCA 480 ACGTCCGCAG CCAAACACGT TCATATTGTT GAGAAGGCAG AGAAATACAA AGTAGGTGGA 540 AGGGTCTCCA CCTACAGCTG TTTTCTGTGG TCTGAGGATT CTTCCCACGT CTTTAATTTC 600 TAGTGCTTTC TAGGGGTCTC AACTTGAACT ATTTAATATT TTCTGGAAGA GAAACATTTT 660 TTGTGGGGGG GGCGGGTGGG GGTGGGACCG AGTCTCGCTC TTGTCTCCCA GGCTGGAGCA 720 CAGTGGCGCG ATCTTGGCTC ACTGCAACCT CCGCCTCCCA GGTTCAAGCG ATTTTCCTGC 780 CTCAGCCTCC CGAGTAGCTG AGATTACAGC GCCCAGCTAA TTTTTGTATT TTTAGTAGAG 840 ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC TAACCTCAGG TGATTCGCCC 900 GCGTCGGCTT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCGCCCG GCCCAGAGGA 960 ACTTTTTTTT TTTTTTTCCA GAGGAACATT TTTTATCCAA AGGAATGACT CCCTAATGGT 1020 GGAATTCCAG GCAATGAAGT GAGGCGCGAG GCAGATTGTC ACATAGGGAG CTGTCATATT 1080 TCATGGGTAC CATTCACGCA AGGCGGGACT TGTTCTTAGG CAGCCAACAC TTCCGCATTG 1140 TCCTGGCATT TGAGCCGCGG AACCAAGTTC CGCGTATCTT GCCCATTGTA ACCCCACAGC 1200 ACCAATTTGA AGCTATGTAG TGCCCTCTGG TGGCCTTCGG TGATTTGGCT TCAGTGTCTC 1260 AAACTCTCTG ATTAGACTGT TTCCAAAGAG AAGGCTGTTA GGGGGCCTCA GAAGTCAGGT 1320 TTGGATGTTT GAGCTCTAAG CTGCAGGATT TGGGGAGCCG TGGTGTGGGG 1370
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