| Tag | Content |
|---|
EnhancerAtlas ID | HS196-12546 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr18:32956120-32957240 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr18:32957027-32957048 | GGGGAAGGACGAGGGGAAGGG | + | 6.31 | | ZNF263 | MA0528.1 | chr18:32957030-32957051 | GAAGGACGAGGGGAAGGGGTG | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGCCATTTG ACTTATTTTC TCACTTCACC AAGTATTGTT CTAGGCCCTG TATAAAGCCT 60
GTGAGTTCAT AAAGTTGTTA CCAAATAAAT GATACAACTT TACACAATGA TGTGCTATGA 120
AACAAACAAT AGCAGACACA CATATTAACA GAATTTACTA TGTGCCAAGC ACTGTTTTGA 180
ACACCTTAGT AAAAATAAAC AAAGGTTAAA TCCTCATAAA AGCCCTAGAT TATTTTTACC 240
CCCATGTTGT AGACGGGGAA GCAGTCACAG CAAAGCCAGG TACTCTGGCC AAGGGCAAAG 300
CTGGGGTCTG AACCCAGGCC GTCCACATTT ATCCATGGTG CTGTGTGGTT AGAGGCCATA 360
GGCAGCAGGG GCCCTTGTGG TGACCCCTGC GCGTTGTCTC AGCGCAGAGG AGGAAGTGGC 420
GGCAGGCAGC CGCGCTCCCA GATGAAGCGG GGCCAGAAGA GTCTGGGGAA CAAGACCTGA 480
GAGGTGGGAA GGGTTGAGGC CACCGGTTTG GAGCCGTCAG GTACCCTAAG GGATATATGA 540
GGGACCCCGG GGCTAAAGCA GCCTCTGGAA GAGAGTGGCC GCCCTGTCAC TTCAGCACCA 600
GGCGCAGAAT CTGTGCTAAA CCTGAGGTGA GGGTAAGGAA CCCCCGACAC CGCACGACAA 660
CCAGAAAGAA CGTCCCTGGA GGGGAGGCTT CGATCAAAGC CTGGGACGCA GGGGTCTTTC 720
TGCAGGGGAC GCCGCTCTCG GCTCTACCCT GCTGTGGTGG GCCGGCTCTG GGAGGGCTGG 780
CTTCCGACCA TCTCCCGACC TCCCGCGCCC ACCGCGCCGC GCCGCGCGCC TCCCAGGCTG 840
GGAACCGCCG GGGCGAAGCG GCAGGTGGCG CGGGTTCACC TGGCAGGGCA GGCGCCCGGG 900
GTCCGCCGGG GAAGGACGAG GGGAAGGGGT GCGCGGACTC AGGGGCAGGC AGCGGAGGGG 960
AGGGGCCTGG GGATCTGGGA CGGTGTAAGG GTGCTGCACT TGCGCGCGAA GGGAGGGGTG 1020
GCGACGAGTC CGCGGCCGCC TCTCCGCGTC CCCCTTCCAC CACCCGGGGA CCACCGCCTC 1080
TGACCGCAGC CTGGGGGCCC TAAAGAGGCC TCGGGTCTCA 1120
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