| Tag | Content |
|---|
EnhancerAtlas ID | HS062-15532 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr8:10785510-10786590 |
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 | chr8:10786282-10786303 | GCCCCCTCCTTCTCCACCTTC | - | 6.33 |
|
| | 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 |
| GH08I010928 | chr8 | 10786021 | 10786311 |
|
Enhancer Sequence | ATCCTTTCCA ACTGCTCCCG GCTCGGTCCC TCCTCTGCTA CTCTTAAGTC CTTGGGTCCA 60
CAGTACACAA CCGAGGGGTA CTGGTTTGCA ATATAATTAG GTCTGGACCC TGGAGGTCTA 120
GTCCAACCCC CACTTTATAG TGGAGGGCCC AGGTGCCAGA ACGCAAGCCA CTGCCGCCTC 180
AGTCACTCAG TGCTGTGGGG CCCGGACGGG ACCAGAATCC AGGCCTGACC CCATGACCTT 240
GCTTGTCCAC CACAACACGT GCAAAGCCCT TGCCTCTCAT GCAGGAGGAT CCTGGCAGCT 300
CCTGCGATCA CGCGGCTGCT GCTGTCCTCG AGGCTCTAGG ATTCTTCCTC CTCCTAGCTT 360
TACCTGGTGT CTGTCTCCCT CAAGATCTAA GGAGCTGCCA AGAAACAACG AGGCAGATGG 420
GTGGGGTGGG AGGAAGGCAT AAGCCATGTC CCCCCTAAAC CCCTGGGCCA GCGCTGCTCT 480
CCCTCGGGAT CTCAGTTTCC TGTGTGTAAA ATCCGGAGCT CCTGGGTGAC CTCTGAGGCT 540
GCGCTGCCAG CCGCCTCCTG CAGAGTCTCC CATCCCCTCT GCAGAAGCGG CCTCGACCCG 600
CGGCCACACG GTGGCGCCAG ACCCTAAGCG TCGCGGAAAC GCCGCTCCAG GCAAGTGATC 660
TCATCCCACA GGCCCGCGCC CTCTTCTGCC AGGGCGCGGA GTGCAAGCCC AGAGGTGCGC 720
TCCGAGGGGG GAACCAAGGC AGGAGACTCA GGATTGGCTG CCATTCCTCC AAGCCCCCTC 780
CTTCTCCACC TTCCAGGCGG GTTCCAGAAA GCTTACCGCA CCGTTCTCCA GGAAGGTATC 840
TCTTGGGAGA GAAGACACCA ACTCTTCTCC CGGACTTGCT CCCAAAGTCG GTGTCACCTC 900
CTGTCACGCC ATATCTGCCC TAAGAGCCTC GGATCATGAA ATACACGGGG GTGAAAGCAG 960
CAACGCCACG TGTCCTCATG GAGCACAGTC TCAAGAAAGC TGGGCCTGGT CTATGGTCTG 1020
CGGGAATGGC CAGTCTTGAG CAAGTCACCT CCCATGGCTG GGCCCCGCTA TTCCCATCAC 1080
|
