| Tag | Content |
|---|
EnhancerAtlas ID | HS150-04238 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr15:79019280-79019950 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr15:79019424-79019434 | GCCCCGCCCC | + | 6.02 | | SP2 | MA0516.2 | chr15:79019754-79019771 | GTCAGTCCCGCCCCTTC | + | 6.22 | | SP4 | MA0685.1 | chr15:79019364-79019381 | CTGGCCACGCCTCCTTT | + | 6.35 |
|
| | 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 |
| GH15I078726 | chr15 | 79019301 | 79019450 |
|
Enhancer Sequence | GCCCCTCTCC CCAAGTGGGC GGGACAGCAG TTGCATGGGC AGCTTTCCTT GTGATGCCAC 60
AGGTTCCTCT GGACACACTG CTGCCTGGCC ACGCCTCCTT TCCCTTTCAT CTTTCTCACT 120
GACCAATGGG CTTGGAGCAT TAAGGCCCCG CCCCATTCTG CATTACAGTG TGGCCCTGGT 180
TACACCTCCT CTGGCTCAGT CACACAGCTG CCTGGTAGGT GACTGGAGGT GTTCGCTGAT 240
GTGGCCCTAA CCCTGCCTCC CTCCCCACCC CACGATGTTA GAAGAAACTC AACAGAGGAA 300
ACTGGCCACA GCCAAGAAAA AAGTAAAACG CATCAGATCA TGGCCCCCCC AACCCAGCCA 360
CAGATCCCCT TTGATGGCAA GACCACTGCC AGAGTCCATA CCAGCCCTTA GGCACACCGG 420
GCTGGGTCCC CCCACACTGG CACCTCTGTG CTCCCTCCAA CCAAAGTCTT GTCAGTCAGT 480
CCCGCCCCTT CAGCAAGCAG CTCAGGCCCT GCCCTCACCA ATCACCCCAG GGTGACTTTG 540
GGCGAGTGAC TTCTGGGGCT CCCGGCTCCA TACTCAGCCT TCACATCCTG CCACCCCAAG 600
CCCGACCTCC CTGAGTTCTT TGGGCTCACC TCTCCAAGGA CCTGGGTCCC CCAGCCCCAG 660
GCCCCACCCT 670
|
