Tag | Content |
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EnhancerAtlas ID | HS193-00261 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:15059380-15060550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr1:15060142-15060156 | CCCCTTTGATGTTC | - | 6.29 | TP63 | MA0525.2 | chr1:15059766-15059784 | AGCAAGTCAGGACAAGTC | + | 6.38 |
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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 |
GH01I014731 | chr1 | 15058041 | 15060857 |
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Enhancer Sequence | GTGACTCAGT GTTCGTTTCA AACTCCTTTA ACCGATAGGT ATTTTCTGAA TGAACAGGGA 60 AATGGAAGCA CATCTTCCCT CCTTCCCCTA TGTTCACGGA GCAAGCAGAA GAGTTTGCTG 120 CATGAGATTT GGGAAGAAAT TCAAAAATGT AGCTCCAAAC AGCTCCCTGG GTGGTTCAGA 180 CATGAGCAAC CACTTTCTTA GAAGACAAGT GCGCTGAGTG TTTCTCGGGG ATCTGTGGCT 240 GCAAAGCGGA TCAGCTCTGA TTTCAGCCCC AGACTTTCTG ACAGAGGGAC TTTCCGCCCA 300 CTGCCCCAGG CTTGGTAATT AAGCAGTCTG AGTGATTGCA GAATTCTCGC ATGTTCCCGG 360 CAGCCTGTGC TTGGAGTTAC CATGAAAGCA AGTCAGGACA AGTCCCAGAG AAACTTAGCT 420 GGTGAAGAGG AAATGGCATT TATTTCAAAT ACACAACCCA GAGTTTGAAG TTGATGAAAT 480 GGGAACAGAG AAGTTCTTTC CCGTTGCCCC ACCCGCCGTG CAATATTGAT TTGCAAATTT 540 TCCAGCAGCC ACCGCCGCTG CAACACTTCA GCAATAGTTG AATTAATGAC CGTGGCAGTG 600 CAGCCTCGTG CCGTAGGGTG GGACCTCCTG GAGCCTTCAG AGTCGGGCAG AGATGCTTCC 660 TGGGAGGTGT CCGGATGACC TCTCTTTCGG GGAGTGGGGG AGTTCTGGAA GTTTCCATAC 720 AAGGAGCAGT TCAAGTGTTG GAGGCCCCCG GTTCTCCCAG GGCCCCTTTG ATGTTCAGCG 780 TGGGGACTCG GGGGTCATAG CAGCTTCCTG GATGTGTCTG AGTCATCAAA GCTCTGCTTA 840 GTAACCTTAA CCTTAGTGCC TTAACCTTGC TAAGGCACAG GTTTCTCGCA TCTGAACCAC 900 CTGCGAGCTG TTTGGGAGCT ACATTTTTGA AGAGGAAACT CCACTTTTAT TCTCTGGGGT 960 TTGGCCCCCC GATCAGCCTC TCCAGATGGG ATCTCCCTCC TTGCCCAATC TGCAGCCCAC 1020 GCCCCAGCCA GTCCAGACTG CTGTCGGTTC CCGGCACACC ATAGGGCTGC GCACAGCTCC 1080 TGCCCTGGCT TCGGCCCTTC CCTCTGCCCA GGATGCCCTT CATCTGGATA TCTACGCCTA 1140 ACAGGTTCAA CTCAGGGGTT CCCTCCTGCC 1170
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