Variant report
| Variant | rs6985650 |
|---|---|
| Chromosome Location | chr8:126643805-126643806 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:126628800-126649400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr8:126638400-126648800 | Weak transcription | Spleen | Spleen |
| 3 | chr8:126639600-126653600 | Weak transcription | Pancreas | Pancrea |
| 4 | chr8:126640800-126649200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 5 | chr8:126640800-126649200 | Weak transcription | NHEK | skin |
| 6 | chr8:126643600-126644200 | Enhancers | HepG2 | liver |
| 7 | chr8:126643600-126644200 | Enhancers | HSMMtube | muscle |
| 8 | chr8:126643800-126644200 | Enhancers | Fetal Lung | lung |
