Tag | Content |
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EnhancerAtlas ID | HS037-09930 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr13:29106330-29107400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NHLH1 | MA0048.2 | chr13:29106871-29106881 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr13:29106871-29106881 | CGCAGCTGCG | - | 6.02 |
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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 |
GH13I028530 | chr13 | 29104923 | 29107883 |
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Enhancer Sequence | AACCCGCAGC TAGCCAAGGG CAAATGCATA CTCGAAAGTG CCACGCCTCT CGTCCACCCT 60 GCGCCGCGTC CAGTCCACCC CCTTCATCCC GCGCCCCATG TCCACCCGCC CGCTGTCCAC 120 CCTGCGCCCC ATGTCCATGC GCCCCCTGTC CACCCGCTCA CTGTCCAACC CGCGCCCCAT 180 GTCCACCCGC CTGCTGCCCA CCCCGCGCCC CCAGTGCACC CGCCCAGCCC CGAGCGCCCG 240 CGGAGCCGAG TGGAGAGCAG CGGCCGCAGC GCGGCGCCAG GCTCGGGCTG GGCTGGCCGG 300 CGCGAACCCC CGGGGGCGTC TGGGCGGCCA GGCCGGGTGG CGGCTGCGCA CGTAGGAGTA 360 CCCCCTGAGC CCAGCCGCTC GGCCGGCCTG ACCCGCGGGT GACCGGATAC GAGTAACGCG 420 TGCGCCCCGA TCTGTGCCCT GCGCGGGGTC GGGCGGGGAC CGGCCGGGGG CGCCGCGCGC 480 CCGGTCGGGT TGACTGTCGG GGGCGATTTC CGCGGGGCAA GGCGGGGGCG CGGGAGCAGC 540 GCGCAGCTGC GGGGCCATTC CACCTGAGCG CCCTGAGGTC AGGGCCGGGG CCTGAGGACA 600 CGGCGCTGGG CTCCGGGGGA CGCGGGTTCA CGCCGGCGCC CGAGCGCCAC CTCCCCGCCC 660 TCCGCCGGCT CACGTAGTCC CGGGGTTCGG TACGTGAAGT GCCGGCGCGA GGCTGCTCAG 720 GCCACCGCAT GGGCCGGGCG ATAAACAATC GCACAGGATA CACAACACCC TGGACTGTCA 780 CAAGCCCCTC GCAGGAAAAG ATAAATAACA TCTGAGGCGC TGCGGCGCGG CTTCCCCGGG 840 CTGAACAAAA ACTAGGAGGT GGGGGGCGGT GGGGCGAAGT AAACAACAGA ACCGAAGAAT 900 TGCCGCACGG AGCCTGGGCC GGCGGAGAAA ATCAGATGCA GTCTCCTTCC CTTTGGTGAC 960 TATCCGTGGG GGTTTCTCCC GGTGGAAATG AGCGACACAC ACACCACACC ACACACTACG 1020 TTCAAACTTT GTCCTTGAAA GCGATAGGCA GCTGCCTCTC TGGGTAAGAG 1070
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