Tag | Content |
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EnhancerAtlas ID | HS098-06777 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr10:43436200-43437720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chr10:43437185-43437197 | CAAGATGGCTGC | + | 6.74 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGACCTCAG ACCTCAGACC ATGGCAGTGT CCGCACGTCC CCACCCCACA CATCCCCACC 60 CTTTCAGAAG AGTCTGCGGG GGGTACAGAG GATGGTCCCA GACTAGAGCT GCAGGACTGT 120 CACAGCCTGC ACATTCCTGC TCCACGCGGG CCCCAGCGCC CCTCAGCTCC AGGCACAGCC 180 CCTGTCCTCG CCTCCCCCGC TTGCCAGGAA ACCGTGGCCC AGCCCGACGT GATTTCCTTT 240 CTCTCAAAGG CTGGCGGCAG CTTTGGCAGC TCAAGGACAG GCCAGGGCAG AAGAAGAGCA 300 GCCTGTCGAA GGCAGCCCTT ATGAATGGGA TCTCATCTGA CTGTAACTGG AATTCGTATG 360 GAGGCTCCGC TTACAGGAAC TTCCCCAGCA GACGAATCTG GGCCACAGAG TTCTGAGCTG 420 GAATGCCCCA GGAGCCAGCC ATAAATCTCC CCAAAATGAG GGTGCACAAT CTCATTGCTC 480 TGGAGGTGCG CTGCTTGCCC CTGGAGACGA CTTGTCATTC TGCGTCCTCC AGGCTCTGCA 540 GAGAGCCAGG AGCCGGGCCA GGGAGAGGTG GATGGGAGTT GGCAAAGTCA CCGTGAAGGT 600 AAACATTTTT ATCATTTAAT TAGGAGCCTC TCAGAAAAGC AAGCTCTGTT TCGTCTAGAG 660 CTGGTCAAAG GAAATGAGAA GTGACATTTT CCCACCCCCA CGTTCCCCTT GGCCCGGGAA 720 ACTCCAAGCT GGAGGCGCGG GATGTGGGCA GCCTCAGGCT GTGCACATCC AGGGCTGGGC 780 CCAGGGGCAG TGGTGGGGCG TGCAGCCTTT GCTGTGCTCT GGCCGTGCCC GGCACTCTCG 840 CTCCCTCATT TGCTCTCATA AACGCCGTCT GCATTATCGA TCACCCTCTG GGTCCCTCCA 900 TAATGCAGGG GCTTCAAACC GCACCCGCTC CTTGAGGGTG CTGCATTCCT GTACTCTCTG 960 CATCTCCCAA GCATATGTGT GACAGCAAGA TGGCTGCAGA TATGCAACTT CCAATAATCA 1020 ATCAACTCTT AAATGATCCT CAATAAACCC TTAAGTAATG ACCAGGAGCC CCTCACCAGC 1080 ATATCTGTAC CCATTTGTTG CTCCATCCAT CCCAATGCAT GACTGACAAG TGTTCACACA 1140 CGTGTCACCC GCAGGCTCCA CTCCAGCTTT GGAGGATGCA GGCAGGACGT CACTCTGGGG 1200 CTCCTGTCTC CTGGGGAGAT GACAGTGAGG GAGGGACACT CATGAAGAAC CTCCCTAGCC 1260 AGTTCCTGAC TCTGCGACTG CCCAGACTCT GAGGGTACTG ACCAACAGAG CTCACTCAGC 1320 TACACAGAGA TGAACCTGGA GGCCTAGAAG AGGCCGGCCT GGCCTGGGTG CAAAGGCCCC 1380 AGGCAGAAGA GCCCAGATGT CCTCACTTCT TTCCCAGTAT GGGGCACCCA AAACATGCAG 1440 CTCCATTTTA ATGAGCAGCT GCTGTCCTTT TTCAGCTGCT ATGGGCCCAC TCTGTCCAGG 1500 CTGCAGCCTC TGGGCAGCCT 1520
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