Tag | Content |
---|
EnhancerAtlas ID | HS177-19277 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr6:35501890-35502630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:35502549-35502567 | CCCTCCCTCCCTCCCTCC | - | 6.03 | ZNF263 | MA0528.1 | chr6:35502545-35502566 | TTTTCCCTCCCTCCCTCCCTC | - | 7.21 | ZNF263 | MA0528.1 | chr6:35502549-35502570 | CCCTCCCTCCCTCCCTCCCCT | - | 7.54 |
|
| 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 |
GH06I035534 | chr6 | 35502201 | 35502350 |
|
Enhancer Sequence | TTCTGCCTCA AGCGATCCAC CCGCCTCAAC CTCCCAAAGC ACTGGGATTA CAGGCGTGAG 60 CCACTGTGCC TGGCTTCCAC CATTGTTATA TATTACATCA ACTGTCTGTT GGGATCTGTT 120 CCTCTTCTGT TTCACTGACA TTTTCATCAT TTTCTTGACC ATTCTTAGAA AGGTGTTGGC 180 AGGGATCAGA GTCTGAAAAC TTTGTCTCTC CTCGTACCCT TGGCCAGACA GGAATCTGTG 240 CTGAAGGTGG TAGCCAAGAT TAGAGTGTGC TCCTGGCAAG ACCCCCTCCT CCTGCCTGTA 300 TGGGGTTGTT TTTGCATTGC ATGATCACAT GCACGCCTCT GCACTCTGCT TTTCTCCCTC 360 ACAACCTTGG CAGCCCCTCA GCCCCACCAC CACTCTGCTG CAGACACGGG ACTAATCTCA 420 TTACTGTCTT TATCCCTGTT CACATCGCCC ATCACAAGAA GCCCAGATCC CTGCTCAGCC 480 CTCCTCCCTG CATCTAATCC CCATCTGGCT CTGCTTCCCT TCTCCCCACC CCCAGCTACT 540 GAAACTCTCT GCCAAGTCCC CGGAACTCAG GCACGGGAGG TCTTCTTTGA ACTCTTCCTT 600 CGCCTTCTGG CTCTTCTGAC ACTGCTTCCC CTACTGTGAG CCCAGGTGGT GACTGTTTTC 660 CCTCCCTCCC TCCCTCCCCT GCCACTGGGC CGGCAGATGG GGGCCCTCCT TGCTCCACTT 720 GCAGAACATG AGCTTCCCCC 740
|