Variant report
| Variant | rs4907006 |
|---|---|
| Chromosome Location | chr1:85271668-85271669 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:85264000-85295600 | Weak transcription | NHEK | skin |
| 2 | chr1:85266400-85287200 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 3 | chr1:85271400-85271800 | Enhancers | GM12878-XiMat | blood |
