Tag | Content |
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EnhancerAtlas ID | HS104-53196 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr6:157637090-157638700 |
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) |
TFAP2C | MA0524.2 | chr6:157637333-157637345 | TGCCCTGGGGCA | + | 6.44 | TFAP2C | MA0524.2 | chr6:157637333-157637345 | TGCCCTGGGGCA | - | 7.22 |
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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 |
GH06I157239 | chr6 | 157636913 | 157640140 |
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Enhancer Sequence | TTTATCAGAG GGAACTTGGC TCCGAATCCA CTTCTGCCTG TCAGTAAGTC AGTTAACTCA 60 TCGTCTTGTG AAATGACTTA TGAACCTCTT TGCCCGGGCT CAGGCGCTGC CCATCTCTAC 120 CCCCAGTGGA AGGGATGGGC ACATGAAGGG AAACAAGTGA GACAACTCGA GACACAAGGA 180 CCTGGGGCTG CGATTGAGAA TAAATGTTTA ACTGGAAAGC GGCTGGGGTG TGGACAAGGA 240 AGCTGCCCTG GGGCAGCATG GGTGAGCTGG GTGCAAGGCC CACACCTGGC ATCACAGCTT 300 CCTGTAGCTC GTCCCAAGGT CCATTACACA CACACACACA CACACACACA CACACACACA 360 CACACACACA CACACACACC CGGAGAGCGG TGACGCGATC TCGGCTCACT GCAACCTCTG 420 CCTCCCAGGA TCAAGCGATT CTCCTGCCAC AGCTTCCCAA GTAGCTGGGA TTACAGGCGC 480 GTGCCACAAT GCCCAGCTAA TCTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCATGTTGC 540 CCAGGCCGAA TTTTGACCTC AGTAAAATTC TGGGGGCACC TGCTGCTTTA AGTGACACTT 600 TGCTTGGCAT GAGTTGCTGA GTGCCTGAGT AGGTTAACAA ATTCAGGCGA ACAAAATCAC 660 CTGCGCTTTG AATGGTGCTA TTATTATATA GGAGTGATTG CTGAGGCCAA GAGAAGGAAA 720 CTCAGAGTTT TTCCAAGGCT CTGCCAGGCT GGGCTGCCCC CACCGGTTTG GGCACTTCTG 780 GCCAGAACCA GTCATCCCCA GAAATGTAGG GCGCAGCTGC TGGACTGTAG GGGAGCCCAG 840 GTTTGGGGAA GAGAAGTGTA TTAGTTTCTG TGGCTGCTGT TACCAATGAC CACAGCCTTG 900 GTGGCTTAAA ACCACAGATG TTCATTCTCT CGTGGCTTGG AGGCCAGAAG CCCTAAACCG 960 AGTGGCCACT GGCAGTGCCT GGCATTCCTT GGCTTGCAGC CACCTCACTC CAGGCTCTGC 1020 CTTAGACTCC ACATGGCTTC CTCCTCTCTG TTCTTCCCTT CTACCTGTCT CAAATCTCCC 1080 TTAGCCTCTC CATTAAAGGA CGCTTGTCAC TGGATTTAGG GCCCACGCAG GTAACCCAGG 1140 ATGATCTCCT CATGTCAAGA TCCTTAATTA TATCTGCAAA GAGCCTTTTT TTCAAATAAG 1200 GTCATATTCA CAGGTTCTAG GGATTAGGAT GCAGACATAC TTTGGGGGCC ACCATTCAGT 1260 ACCCCACAGG AAGCACAGGG CAGCAGCCGG CTTGGCCCGC AGTGCTCCTC CCGAGCCTGC 1320 TTCATTAATG GGCTGGTGCT TCGTCAACAC GACAGCATTT GCCAAGGGCA GGTGTCCTTT 1380 TCTCCATCCC ACCTTGGAAG CCTCCCAGAA GCGGCCAGGC CCCTGTGGGA CTGCCCCCAC 1440 TGCAGCGTCT ACCTCCATAA ACACTTCCCG GGATCCCCCT TGGAAACCTG GCTGCCTGGC 1500 TCCCCTCCCT CCACCCTCTT CCTCAGCAAT TACCCCAAGC TGGCCGGCTG CAAGGTGCTG 1560 GGGATCCCCG GGAGTAGGGG GCTGGAGCCC GGTTCAGCCA GGCCCTCCCC 1610
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