Variant report
| Variant | rs10485153 |
|---|---|
| Chromosome Location | chr6:134069098-134069099 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:134063000-134069800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 2 | chr6:134063000-134070800 | Weak transcription | Right Atrium | heart |
| 3 | chr6:134063000-134073000 | Weak transcription | Fetal Kidney | kidney |
| 4 | chr6:134065800-134070000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 5 | chr6:134067200-134072800 | Weak transcription | Osteobl | bone |
| 6 | chr6:134067600-134075000 | Weak transcription | Stomach Mucosa | stomach |
| 7 | chr6:134068000-134073000 | Weak transcription | A549 | lung |
| 8 | chr6:134068600-134071000 | Enhancers | Fetal Stomach | stomach |
| 9 | chr6:134068600-134082200 | Weak transcription | Aorta | Aorta |
| 10 | chr6:134068800-134069800 | Enhancers | Fetal Lung | lung |
| 11 | chr6:134068800-134070400 | Enhancers | NHLF | lung |
