Tag | Content |
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EnhancerAtlas ID | HS088-26533 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr19:6862600-6863980 |
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 | GGCTCATGCC TATAATCCTA GCACTTTGGG AGGCCGAGGC AGGTGGATCA CTTGAGCTCA 60 GGAGTTCGAA ACCAGCCTGG CCAACATGGT GAATGTACAA CGGACAGCCC CCAATACAGA 120 CAGACAGACA CACACACACA CACACACACA CACTCACTCA CTCCTACCCC CAGCCCTAAG 180 AATTTACAAA CACTGATAAA GACAAATGAA ATCAGCGGAT ATAGACTTCA AACGCCGTCA 240 GACAGACACC CACTAGATCA AACAGGGACA TTCCTAAACA TCACACAGAC ACATCGCCAG 300 GCAGTCCCAC CGCAGACAGC CACAAATTAA AGCCGCGCTT GCCCCCTGAT GGACAGCAGC 360 AGTAGTGCGC CACCTCGATA GCGCAATCTC CCAGAGCGCT GGCATTGCAG GCGTGAGCCA 420 ACGTCCGCAG CCAAACACGT TCATATTGTT GAGAAGGCAG AGAAATACAA AGTAGGTGGA 480 AGGGTCTCCA CCTACAGCTG TTTTCTGTGG TCTGAGGATT CTTCCCACGT CTTTAATTTC 540 TAGTGCTTTC TAGGGGTCTC AACTTGAACT ATTTAATATT TTCTGGAAGA GAAACATTTT 600 TTGTGGGGGG GGCGGGTGGG GGTGGGACCG AGTCTCGCTC TTGTCTCCCA GGCTGGAGCA 660 CAGTGGCGCG ATCTTGGCTC ACTGCAACCT CCGCCTCCCA GGTTCAAGCG ATTTTCCTGC 720 CTCAGCCTCC CGAGTAGCTG AGATTACAGC GCCCAGCTAA TTTTTGTATT TTTAGTAGAG 780 ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC TAACCTCAGG TGATTCGCCC 840 GCGTCGGCTT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCGCCCG GCCCAGAGGA 900 ACTTTTTTTT TTTTTTTCCA GAGGAACATT TTTTATCCAA AGGAATGACT CCCTAATGGT 960 GGAATTCCAG GCAATGAAGT GAGGCGCGAG GCAGATTGTC ACATAGGGAG CTGTCATATT 1020 TCATGGGTAC CATTCACGCA AGGCGGGACT TGTTCTTAGG CAGCCAACAC TTCCGCATTG 1080 TCCTGGCATT TGAGCCGCGG AACCAAGTTC CGCGTATCTT GCCCATTGTA ACCCCACAGC 1140 ACCAATTTGA AGCTATGTAG TGCCCTCTGG TGGCCTTCGG TGATTTGGCT TCAGTGTCTC 1200 AAACTCTCTG ATTAGACTGT TTCCAAAGAG AAGGCTGTTA GGGGGCCTCA GAAGTCAGGT 1260 TTGGATGTTT GAGCTCTAAG CTGCAGGATT TGGGGAGCCG TGGTGTGGGG GTGATTTATT 1320 TATTTATTTT TGAGAAAGAG TCTCACTCTG TCGCCCAGGC TGGAGGGCAA TGGTGTGATC 1380
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