Variant report
| Variant | rs7518985 |
|---|---|
| Chromosome Location | chr1:220686705-220686706 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:220683200-220689800 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 2 | chr1:220685200-220689400 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 3 | chr1:220685400-220687000 | Weak transcription | Placenta | Placenta |
| 4 | chr1:220685600-220687800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 5 | chr1:220685600-220689000 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
| 6 | chr1:220685600-220689000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
| 7 | chr1:220685600-220689200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
| 8 | chr1:220685800-220686800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 9 | chr1:220685800-220687400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 10 | chr1:220685800-220689400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 11 | chr1:220686000-220687200 | Weak transcription | HMEC | breast |
| 12 | chr1:220686200-220687200 | Weak transcription | NHEK | skin |
