Tag | Content |
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EnhancerAtlas ID | HS105-36374 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr17:80710250-80711700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR1 | MA0162.3 | chr17:80710252-80710266 | GGTGCGTGGGCGGC | - | 6.06 | EGR2 | MA0472.2 | chr17:80710254-80710265 | TGCGTGGGCGG | - | 6.32 | EGR3 | MA0732.1 | chr17:80710252-80710267 | GGTGCGTGGGCGGCG | - | 6.46 | NKX2-5 | MA0063.2 | chr17:80711560-80711570 | CTCAAGTGGT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGGTGCGTG GGCGGCGCCG CGTGCCCGCT TCCTCCCCCG GCCCGGGTTC GGCGCGCTGA 60 GTGCACTTTA CCGGGCGGGG ACCGCAGCCC GGCGGCGCCG GCCGCTCTGC GAGGGCTGCC 120 GGTGCGCGGT CCCGCGGGCC GTGGTGGGGC GCGGCCTTCC TAGGCGGGAG AGGGCCACCC 180 CGGCGCGGCG TTAGGTGCAC GGGGCAGACG CGCGCCTCCC TTGGGGGGAC CGTGGCCCGC 240 GGAGCGCCTG CTCTCGCACG GGGTGAAGCC TCTGCGGCCT CCCCGGGAGG CGGGGTGCAG 300 AAGCCCTCCG TCCCCCGTCT CCGTCACTGG AGGAGGTCCC TGGGCTGGGG AGACTCGGGC 360 CAGACCCCTC CGGACAGCTG GTCAGCCCTG CAGTGTGGAC TCCCAGGCTT GCCTCCACCG 420 AGCGCGGTTT CTGTGAATGT TGTGTGGACA GGGAGATAGG GAATGAGAGA GGGGGACGCA 480 GGGAACAAAC CTGCTGCAAA CAAAGCGCGC CTCGGGTGGG GAGGGCAGCA GCCTGTCCGT 540 TCCGTGGACG CCGTGGACAG AGCGGGCTGG CCGGGTCCGT GCCTCTGCAG GCGGGGTGGG 600 GTGTAGGTAC CCCTGTGGAG GCCATTCGAT GAGTCTAAAT TCTCCGAGTT CAGACCCACC 660 TTTACCGCTG TCTATAATGG GTTATTTCCA AACAAGTCCT TAGGAGCTCA TAGCTAAGTA 720 GTTACATGGG GTTTTGTAAT TCAGTAAAAT CATCTTTGTA GACCCTTTGA GTAAGAAGAA 780 CTTTTGCATT ATTTGGCCTT CCTCATTTTA GAATGACAGC GCTTTGATTT TAGGAGTCAG 840 GCAGGGTGGG GGGCCTTGTG GGAGGAGTGC GGGTTCGGCG TCAGATCCTC CTGCCTGTGA 900 ATTCTGGCCC TGTCGCTTGG ACCTGATACT TGATTGCCTG TTTCTTCGGG TGTAAGCTGG 960 GGCGGATAAC GATGCCTCTC GTGCAGAACT GTTCTGAGGG TGAGGGACCC TCATCCAGGG 1020 ACCAGTGAAG CCAGATTTTT TGTTCCTGGT GTAACAGCCC AATGGCTTCT TCCTTTTTTT 1080 TTTTTTTTTT TTTTTGATAC GAAGTCTTGC TCTGTTGCCC AGGCTGGAGT GCAGTGCAGT 1140 GGTGCGATCT TGGCTCACTG CAACCTCAAC CTCTCAGGTT CAAGCTATTC TCCTGTCTTA 1200 GCCTCCCGAG TAGCTGGGGC TACAGGCGCG CGCCACCACG CCCGGCTAAT TTTGTATTTT 1260 TAGTAGAGGG GGTTTCACCA TGTTGGTCAG GCTGGTCTCA AACTCCTGAC CTCAAGTGGT 1320 CGCCCGACTC AGCCTCCCAA AGTGTTGAGA TTACAGGTGT GAGCCACTGC GCTCGGCCCC 1380 AGTGGGTTCT TTCTGCGGGC TGCCCAGATA GAGTTGATTT GTCAGGGCAG GGGAGTTGCC 1440 ATGGAGAAGA 1450
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