| Tag | Content |
|---|
EnhancerAtlas ID | HS139-52525 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:10785700-10786610 |
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 | TGCTGTGGGG CCCGGACGGG ACCAGAATCC AGGCCTGACC CCATGACCTT GCTTGTCCAC 60
CACAACACGT GCAAAGCCCT TGCCTCTCAT GCAGGAGGAT CCTGGCAGCT CCTGCGATCA 120
CGCGGCTGCT GCTGTCCTCG AGGCTCTAGG ATTCTTCCTC CTCCTAGCTT TACCTGGTGT 180
CTGTCTCCCT CAAGATCTAA GGAGCTGCCA AGAAACAACG AGGCAGATGG GTGGGGTGGG 240
AGGAAGGCAT AAGCCATGTC CCCCCTAAAC CCCTGGGCCA GCGCTGCTCT CCCTCGGGAT 300
CTCAGTTTCC TGTGTGTAAA ATCCGGAGCT CCTGGGTGAC CTCTGAGGCT GCGCTGCCAG 360
CCGCCTCCTG CAGAGTCTCC CATCCCCTCT GCAGAAGCGG CCTCGACCCG CGGCCACACG 420
GTGGCGCCAG ACCCTAAGCG TCGCGGAAAC GCCGCTCCAG GCAAGTGATC TCATCCCACA 480
GGCCCGCGCC CTCTTCTGCC AGGGCGCGGA GTGCAAGCCC AGAGGTGCGC TCCGAGGGGG 540
GAACCAAGGC AGGAGACTCA GGATTGGCTG CCATTCCTCC AAGCCCCCTC CTTCTCCACC 600
TTCCAGGCGG GTTCCAGAAA GCTTACCGCA CCGTTCTCCA GGAAGGTATC TCTTGGGAGA 660
GAAGACACCA ACTCTTCTCC CGGACTTGCT CCCAAAGTCG GTGTCACCTC CTGTCACGCC 720
ATATCTGCCC TAAGAGCCTC GGATCATGAA ATACACGGGG GTGAAAGCAG CAACGCCACG 780
TGTCCTCATG GAGCACAGTC TCAAGAAAGC TGGGCCTGGT CTATGGTCTG CGGGAATGGC 840
CAGTCTTGAG CAAGTCACCT CCCATGGCTG GGCCCCGCTA TTCCCATCAC AGGAGGGGCA 900
GGCAGGAGGG 910
|
