Variant report
| Variant | rs57600468 |
|---|---|
| Chromosome Location | chr9:93855420-93855421 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:93847800-93855600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr9:93852600-93859800 | Weak transcription | Fetal Heart | heart |
| 3 | chr9:93852600-93861600 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 4 | chr9:93852800-93861200 | Weak transcription | NHLF | lung |
| 5 | chr9:93853200-93857800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 6 | chr9:93854200-93860600 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
| 7 | chr9:93855400-93855800 | ZNF genes & repeats | Fetal Intestine Small | intestine |
