| Tag | Content |
|---|
EnhancerAtlas ID | HS041-01187 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr1:54602960-54604160 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:54603708-54603729 | GGGGGAGGGAGGTGAGGTGGA | + | 7.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I054134 | chr1 | 54600550 | 54604344 |
| Enhancer Sequence | GGGGGAGGGG GCAATAAATG TAAAATACAC CCACGTGTCA GCGTGCCCCA AAGGAAAATC 60
TAGCAAAGAA GAAACAGCGG GAGAGTAGAG CGAATCGGAA CTGGGGAGGA ATGAGGAAGG 120
AGAGCTTCAG TTTTAAAAAG GGTGGTAAGG GAAGCCTCAC TTTCCCTCCC TACAATGACC 180
CCAGGAGGTG GATGTGACTA AACTCATTTT ACAGGTTTGG AAATGGATGC TCTGAGAGAT 240
GAAGTTGTTT GCAGTGGCCA ACCGGGTCGA CAGGATTTCA GAGTTCGTGG TCTGTTTGCC 300
CTATTCAGCA GGCTCCTGCA GCCCTCCTGG CCAGGACAGT GTGCACATGA CTCAAAATGT 360
CTGCTTTGGG TGAGCATGTG TGTGTGTGTG TGTGTGCGTG TGTGTGTGTG TGTGTGTGCA 420
TGCGGGGGCA GGGGTGAGGA TAGGGGAAAT GAAGGCAACT GCCTGGTGGG AGGAAAAGGA 480
AAGAGAGCTG GCAGGCAGAG GCCTGGAACT CTCAACCCCT CTCCGGGAAA TGCCTCAGAC 540
ATATTTCAGC CTCTGGTGTC TGGGCAGTCG GGGATTTATG GGCCAGCCAT CTCCCACGAT 600
GATCTCGGTG GTGCTGAACT GTGTGTCACC CCCAGCTGGC ACTGTGGCTG CCCTCCCAGT 660
GGGGAGGCCT CCTGCAGCCT GGGCCACATC TGGAGCCTCG CCCAGTGTGA GTGCCCTTGT 720
CTGCCCCTGG GCCCCCACAA GGATCTGAGG GGGAGGGAGG TGAGGTGGAG TGGGGGGTGG 780
GCACTCCTGC CCCGAAGCCC CTGGAACAGG AGCTGGGATA AGAACCCCCG CTAACTTCCT 840
CTCCTTCTCT GCAGAAGGGG CTTGTCCTAA ATCACACAGG GCTGGGAGAG GGCCTGGGAG 900
AGTTCTGGAA ATAAGACTAT CAGAGGCAAA AGGAACTTTA AAGATCTTTC TGTCAATATC 960
CTCATCTTAC AGGTGGAGAA ACTGAGGCCC ACAGAGACAT GGGGCCATGC CAGCTAGTGG 1020
AGGCATAGCC AATGGAGCTG GGCTCTCCAG GGCTGTGCTA ACAGAGCCAC AGCTCTCCCA 1080
CCCCAGCTTG CATGTGGAGC CCACTAAGGC CCGAAGGGGC TGGCCTGCCC AAGTTCACGG 1140
CTCTGCCGCA AGCTTGCTGC AGATCACCAT CTCCTCCATT CCTGGCCCCA ACTCCCCTTG 1200
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