Variant report
Variant | rs147793252 |
---|---|
Chromosome Location | chr2:185512791-185512792 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:185511200-185519600 | Weak transcription | Muscle Satellite Cultured Cells | -- |
2 | chr2:185511400-185513200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
3 | chr2:185512600-185512800 | Enhancers | Fetal Intestine Small | intestine |