| Tag | Content |
|---|
EnhancerAtlas ID | HS080-23766 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr3:52816280-52816970 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr3:52816651-52816672 | TGCCCTGTCCATGGTGCAGTG | - | 6.16 | | ZNF263 | MA0528.1 | chr3:52816788-52816809 | TCTCCACCTCCCTCATCCACC | - | 6.03 | | ZNF263 | MA0528.1 | chr3:52816785-52816806 | CCTTCTCCACCTCCCTCATCC | - | 6.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGGTAGGCT GCAGCTTGAA ACAGCTCACC CAGCAGAAGC TTCCACAGCC CCATCACTCA 60
CCACATGCCA GTTTTGCTGC CAGAGTCTGG TTTGGGATTT ATCCTCCTGG TCAGAGGCAG 120
AGTGATTTAA CAGGAAATCC CAGTGGTTAG CATCTCTGGA ATCAGCATCG CTTCCTCACT 180
GTGCAGTCGT GAGGAAGTGC ATTCACCTCT CCTCAATGGC AAAAAATGGG AATGACAATG 240
GTGTCTGCAG GGTCATGGAG TTACCCCCTG GGGGAAGTGC TTAGAAGAGG AAACCTGTGC 300
ACTACAATTA CGGTGGTCCG TGGGGAGGCA TCTTATAGCA GGGAATAGCT CTCCGCCCAC 360
AGGGTTTGGA GTGCCCTGTC CATGGTGCAG TGTAGACATG GCTGGACAAG GAGTATTCTA 420
GAAGCACAGC TCCTGGGGTC CTTTCTCTTA ATCCTGCCCC TCCCGAACTC CTGATTATTT 480
CTTTTCCCCA TGGTGGGTTC CTTTGCCTTC TCCACCTCCC TCATCCACCC CAAGGCCCGG 540
CAGGATGCTC CTGTCTCGGG GCCACCTGGT TGTCCTATCT CCTCCTGCTT GTCCACCCTG 600
TGGATCTCTG AAATGGGTAT TTGGAGTTGG AAGGTGCTGT CCTGGGGCCA CCCTGGGGCC 660
CTGTCTGTCT ACTGACTGTT CTGTCCTTGC 690
|
