| Tag | Content |
|---|
EnhancerAtlas ID | HS127-14363 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr18:32956080-32957240 |
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 | AAAATCTTAC GTGCGCCTCC GTCTTCCATC GTTATGTATC CTGCCATTTG ACTTATTTTC 60
TCACTTCACC AAGTATTGTT CTAGGCCCTG TATAAAGCCT GTGAGTTCAT AAAGTTGTTA 120
CCAAATAAAT GATACAACTT TACACAATGA TGTGCTATGA AACAAACAAT AGCAGACACA 180
CATATTAACA GAATTTACTA TGTGCCAAGC ACTGTTTTGA ACACCTTAGT AAAAATAAAC 240
AAAGGTTAAA TCCTCATAAA AGCCCTAGAT TATTTTTACC CCCATGTTGT AGACGGGGAA 300
GCAGTCACAG CAAAGCCAGG TACTCTGGCC AAGGGCAAAG CTGGGGTCTG AACCCAGGCC 360
GTCCACATTT ATCCATGGTG CTGTGTGGTT AGAGGCCATA GGCAGCAGGG GCCCTTGTGG 420
TGACCCCTGC GCGTTGTCTC AGCGCAGAGG AGGAAGTGGC GGCAGGCAGC CGCGCTCCCA 480
GATGAAGCGG GGCCAGAAGA GTCTGGGGAA CAAGACCTGA GAGGTGGGAA GGGTTGAGGC 540
CACCGGTTTG GAGCCGTCAG GTACCCTAAG GGATATATGA GGGACCCCGG GGCTAAAGCA 600
GCCTCTGGAA GAGAGTGGCC GCCCTGTCAC TTCAGCACCA GGCGCAGAAT CTGTGCTAAA 660
CCTGAGGTGA GGGTAAGGAA CCCCCGACAC CGCACGACAA CCAGAAAGAA CGTCCCTGGA 720
GGGGAGGCTT CGATCAAAGC CTGGGACGCA GGGGTCTTTC TGCAGGGGAC GCCGCTCTCG 780
GCTCTACCCT GCTGTGGTGG GCCGGCTCTG GGAGGGCTGG CTTCCGACCA TCTCCCGACC 840
TCCCGCGCCC ACCGCGCCGC GCCGCGCGCC TCCCAGGCTG GGAACCGCCG GGGCGAAGCG 900
GCAGGTGGCG CGGGTTCACC TGGCAGGGCA GGCGCCCGGG GTCCGCCGGG GAAGGACGAG 960
GGGAAGGGGT GCGCGGACTC AGGGGCAGGC AGCGGAGGGG AGGGGCCTGG GGATCTGGGA 1020
CGGTGTAAGG GTGCTGCACT TGCGCGCGAA GGGAGGGGTG GCGACGAGTC CGCGGCCGCC 1080
TCTCCGCGTC CCCCTTCCAC CACCCGGGGA CCACCGCCTC TGACCGCAGC CTGGGGGCCC 1140
TAAAGAGGCC TCGGGTCTCA 1160
|
