Tag | Content |
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EnhancerAtlas ID | HS105-52916 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:31198100-31199580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr22:31198912-31198933 | GACGCTGTCCGCGGTGCTGAA | - | 9.24 | ZNF263 | MA0528.1 | chr22:31198220-31198241 | GGAGGAGGAGGCGTGGGAGGG | + | 7.02 |
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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 |
GH22I030802 | chr22 | 31198164 | 31200587 |
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Enhancer Sequence | CCCCACCCCA CCCTCATGTT TCAGAGGAGA AACTGAGGCT CAGGTGGCCT GGGTCATGTT 60 GCTGGTCTGT GGCAGAAGCC AAGTCAGAAT CAATGACCCC CCAGGGACTT TCCTGGCTGG 120 GGAGGAGGAG GCGTGGGAGG GATTTGAATA GAATGTGGAA GCGGTTCTGC GAGATGTCAT 180 CAGGCTCTAG CAGTCCCGTC TGTTGGTTGG TGCTGGGAGA GGGAATTGGA TTCCAAGTGG 240 GGATGGGACC GCATCTCCCC TAGTTCCCGA GATAGACTCG CCTGTAACTG GATCACTCCT 300 TGCAACCTCG GGTAGCGTGT GACTGGAGAA ATGAGGGCTG GAGCCGTGGA CCATCCGAGG 360 GCCCCTCCCC TGCTGGGTCC AGGCAAAGGG CCGGCCCTCT CCAGCCTCGA TTGGGGCGCG 420 ATAGCGCCCT TAGTGTCGTG TCGGGTTCCA GGCCACGCTC GGGCATTTTA AGAGGCTGAG 480 GTGCGCCTTC CGCTGCCCGC CTGCGTCCCG CCACGGAGAG CTCGCCTTTA TCTAGCCCTC 540 TGGGCGAGAG AAGAAGGCTA ATCCCAGCCT GGGACAAGGC TGGCTGAGGC GTGCCGGATC 600 CTCCGGGGAC CGATCGGTGG CCTCGCGCGG CTCTCATCGC TCTCCGAGCA GTGCTCCAGG 660 GGGCGGAGGG AGCCTCCTCG GGCGGTGGGG AGGAGGCTGG AGGAATGAGG ACGCAGCACG 720 GCGCGCCCTT GCAGCGCTCA GGCTGACGGG CGGGCGGGCG GAGCGGGCGC ACGGCTCCTC 780 TAGGTCCGGC TGCTCTCTGA GCTCGCGGGC TGGACGCTGT CCGCGGTGCT GAAGCGGCGC 840 CCGCGGCAGG GAGGCGGACC CGGAGCCGCC GGGCAGCACA CACCCAATCC CGGGACCGCC 900 CTCCTCCCAG GCTCGGAGAG GCGGTGGCAG CCGGCACTGC ACCCAGATGG ACTGAGAGCG 960 CGGCGGCGGG AAGGCGGCGG CGGCGGCGGC AGCAGCAGCA GCTGCAAGAG CCCTCGCAGC 1020 CTCGGGGCAG GACCCACGTC CACACCCGAG AGCCCCTCCC TGGGGTGAGT CAGGGCGGGC 1080 GGAAGAGGGA TGGGGTGGAC GGGTCCTGGG GCATGGGATC TCTTGGGCTT TAAAATTTCC 1140 CTTCCCCGTT GTAAATTTCT TCCAGCCCAG ATCTTGAGCA GCTTTCAGGG CTGAGGGCTC 1200 AGAGCTATGC CTCAGCACTT TCCCAGTCCT GGGATAGAGG GCAGGCCCCT CTGCCCTCAC 1260 AAGCCAGGGG ACAAAGGGTT TAGCCAGAAG CCAGACAGTC ACAAGGCATG TCCTCCTCTC 1320 CACCTTGGGT GCAGCCCACA ACAAGGTACC AGGAAAAGCT GTTTGCCCAG GCTGGTGCCA 1380 CAGGGGGGAC AGCTTCCCGT CTCTGGTCTC TGTTCAGAGG CCTGGCCCCG AGCAACCTAG 1440 CCACTGGAAT TCAGCCCAGA CAGAGGCCAG CCATCTTTTA 1480
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