| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00384 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr1:54602740-54604110 | 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 | TTGGCAGGCC CAGTGAATGC TGAGTGAATG AATGAATGTT CTTAATAATT ATAAAAATTC 60
ATCTGCTAAT CACTTGGCCA TGTGCCAGGC AATTCATTCA ATTATTTAAC AAATATATTG 120
ATGGCCTGCT ATGTTCAGGT CCTATTCTCA GCACCACAAA TACAAAAATG AGGAAAAAAC 180
ACAGCTGAAA TTCTTGCCTT GTGGAGCTTA CATTCTAGAT GGGGGAGGGG GCAATAAATG 240
TAAAATACAC CCACGTGTCA GCGTGCCCCA AAGGAAAATC TAGCAAAGAA GAAACAGCGG 300
GAGAGTAGAG CGAATCGGAA CTGGGGAGGA ATGAGGAAGG AGAGCTTCAG TTTTAAAAAG 360
GGTGGTAAGG GAAGCCTCAC TTTCCCTCCC TACAATGACC CCAGGAGGTG GATGTGACTA 420
AACTCATTTT ACAGGTTTGG AAATGGATGC TCTGAGAGAT GAAGTTGTTT GCAGTGGCCA 480
ACCGGGTCGA CAGGATTTCA GAGTTCGTGG TCTGTTTGCC CTATTCAGCA GGCTCCTGCA 540
GCCCTCCTGG CCAGGACAGT GTGCACATGA CTCAAAATGT CTGCTTTGGG TGAGCATGTG 600
TGTGTGTGTG TGTGTGCGTG TGTGTGTGTG TGTGTGTGCA TGCGGGGGCA GGGGTGAGGA 660
TAGGGGAAAT GAAGGCAACT GCCTGGTGGG AGGAAAAGGA AAGAGAGCTG GCAGGCAGAG 720
GCCTGGAACT CTCAACCCCT CTCCGGGAAA TGCCTCAGAC ATATTTCAGC CTCTGGTGTC 780
TGGGCAGTCG GGGATTTATG GGCCAGCCAT CTCCCACGAT GATCTCGGTG GTGCTGAACT 840
GTGTGTCACC CCCAGCTGGC ACTGTGGCTG CCCTCCCAGT GGGGAGGCCT CCTGCAGCCT 900
GGGCCACATC TGGAGCCTCG CCCAGTGTGA GTGCCCTTGT CTGCCCCTGG GCCCCCACAA 960
GGATCTGAGG GGGAGGGAGG TGAGGTGGAG TGGGGGGTGG GCACTCCTGC CCCGAAGCCC 1020
CTGGAACAGG AGCTGGGATA AGAACCCCCG CTAACTTCCT CTCCTTCTCT GCAGAAGGGG 1080
CTTGTCCTAA ATCACACAGG GCTGGGAGAG GGCCTGGGAG AGTTCTGGAA ATAAGACTAT 1140
CAGAGGCAAA AGGAACTTTA AAGATCTTTC TGTCAATATC CTCATCTTAC AGGTGGAGAA 1200
ACTGAGGCCC ACAGAGACAT GGGGCCATGC CAGCTAGTGG AGGCATAGCC AATGGAGCTG 1260
GGCTCTCCAG GGCTGTGCTA ACAGAGCCAC AGCTCTCCCA CCCCAGCTTG CATGTGGAGC 1320
CCACTAAGGC CCGAAGGGGC TGGCCTGCCC AAGTTCACGG CTCTGCCGCA 1370
|
| |
|
|
|
