| Tag | Content |
|---|
EnhancerAtlas ID | HS051-26929 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:144976570-144977240 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:144976844-144976863 | TGCTGCCATCTGCTGGGGA | - | 6.3 |
|
| | 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 |
| GH08I143902 | chr8 | 144976568 | 144977169 |
|
Enhancer Sequence | AATGTTTCCA AACCCTTCTG CCTGCAACCG CCGTCCTGGG GATGAGAAAT CTCTGGGGAG 60
GAGGAGTTTG GGGGCCAGCA TCTTGTGTCG GGGCATGGGT TGTTGAGATG ACGCTAGCAC 120
CCCCCATCCC CCGCCCCTGC CTACTGGGCT GGTTTCCCCT CCAGGGGGTG AGGTGGCGCC 180
TCCCAGATGG GACACAGCCT GCTGTCCCCA CTTTAGTCAG AAAGCAGGAG TGAGACAGGT 240
GGCCGGGACG AGACGCTGGG GCTGGTAGGC GCTTTGCTGC CATCTGCTGG GGAGCCCGCA 300
GCAGCCGCCG CCGTGGACCT TGTGCTGGTG GAAAGCACAA AACCACTGTC CACGTGAAGG 360
CCGCCCATGT CCTGGCAGCG CCCCTGAGGG GTGGCCTCCT GCAACCACCC ACCTGCAACC 420
ACCCACCTGC AACCACCCAG GGGGCTGCAA AGCCACTCTG CTCGTGCTGG CCTGGCCTCT 480
GAACCTATCA CAACATAAGA CAGAAGAGGA CTGAATGGGG TGCGGCCCAG CGTACGCTGC 540
TCAGCCTGGT CTTCGTGAAT GGGCTCCATC CAGCCTCTGT CCTCAGAGAC GGCAGGTGGT 600
GCCTCATCTT CCTGGCAGAC CTGGAGGGAG TGTGGGTAGA GTGGGACCCA GCCAGGAGTC 660
CAGGCCCTGA 670
|
