Variant report
| Variant | rs16925030 |
|---|---|
| Chromosome Location | chr11:34026283-34026284 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:34020400-34028000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr11:34025200-34029000 | Enhancers | Duodenum Mucosa | Duodenum |
| 3 | chr11:34025400-34026600 | Enhancers | Fetal Intestine Large | intestine |
| 4 | chr11:34025400-34026800 | Enhancers | Fetal Intestine Small | intestine |
| 5 | chr11:34026000-34026400 | Enhancers | HepG2 | liver |
