Variant report
| Variant | rs1267720 |
|---|---|
| Chromosome Location | chr6:16065812-16065813 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:16059200-16082600 | Weak transcription | Right Atrium | heart |
| 2 | chr6:16060600-16069600 | Weak transcription | Fetal Brain Male | brain |
| 3 | chr6:16062400-16066000 | Weak transcription | NHEK | skin |
| 4 | chr6:16063400-16066200 | Enhancers | H9 Cell Line | embryonic stem cell |
| 5 | chr6:16064200-16066000 | Enhancers | ES-WA7 Cell Line | embryonic stem cell |
| 6 | chr6:16064400-16066200 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 7 | chr6:16065000-16066200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
| 8 | chr6:16065000-16066200 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 9 | chr6:16065000-16069800 | Weak transcription | Fetal Brain Female | brain |
