| Tag | Content |
|---|
EnhancerAtlas ID | HS029-07160 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr18:32956180-32957240 |
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 | GTGAGTTCAT AAAGTTGTTA CCAAATAAAT GATACAACTT TACACAATGA TGTGCTATGA 60
AACAAACAAT AGCAGACACA CATATTAACA GAATTTACTA TGTGCCAAGC ACTGTTTTGA 120
ACACCTTAGT AAAAATAAAC AAAGGTTAAA TCCTCATAAA AGCCCTAGAT TATTTTTACC 180
CCCATGTTGT AGACGGGGAA GCAGTCACAG CAAAGCCAGG TACTCTGGCC AAGGGCAAAG 240
CTGGGGTCTG AACCCAGGCC GTCCACATTT ATCCATGGTG CTGTGTGGTT AGAGGCCATA 300
GGCAGCAGGG GCCCTTGTGG TGACCCCTGC GCGTTGTCTC AGCGCAGAGG AGGAAGTGGC 360
GGCAGGCAGC CGCGCTCCCA GATGAAGCGG GGCCAGAAGA GTCTGGGGAA CAAGACCTGA 420
GAGGTGGGAA GGGTTGAGGC CACCGGTTTG GAGCCGTCAG GTACCCTAAG GGATATATGA 480
GGGACCCCGG GGCTAAAGCA GCCTCTGGAA GAGAGTGGCC GCCCTGTCAC TTCAGCACCA 540
GGCGCAGAAT CTGTGCTAAA CCTGAGGTGA GGGTAAGGAA CCCCCGACAC CGCACGACAA 600
CCAGAAAGAA CGTCCCTGGA GGGGAGGCTT CGATCAAAGC CTGGGACGCA GGGGTCTTTC 660
TGCAGGGGAC GCCGCTCTCG GCTCTACCCT GCTGTGGTGG GCCGGCTCTG GGAGGGCTGG 720
CTTCCGACCA TCTCCCGACC TCCCGCGCCC ACCGCGCCGC GCCGCGCGCC TCCCAGGCTG 780
GGAACCGCCG GGGCGAAGCG GCAGGTGGCG CGGGTTCACC TGGCAGGGCA GGCGCCCGGG 840
GTCCGCCGGG GAAGGACGAG GGGAAGGGGT GCGCGGACTC AGGGGCAGGC AGCGGAGGGG 900
AGGGGCCTGG GGATCTGGGA CGGTGTAAGG GTGCTGCACT TGCGCGCGAA GGGAGGGGTG 960
GCGACGAGTC CGCGGCCGCC TCTCCGCGTC CCCCTTCCAC CACCCGGGGA CCACCGCCTC 1020
TGACCGCAGC CTGGGGGCCC TAAAGAGGCC TCGGGTCTCA 1060
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