Variant report
| Variant | rs2683682 |
|---|---|
| Chromosome Location | chr2:67729163-67729164 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:67725400-67729200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 2 | chr2:67726000-67729800 | Weak transcription | Placenta | Placenta |
| 3 | chr2:67726400-67730000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 4 | chr2:67728000-67729800 | Weak transcription | Ovary | ovary |
| 5 | chr2:67728200-67729400 | Weak transcription | NHLF | lung |
| 6 | chr2:67728200-67742800 | Weak transcription | Fetal Lung | lung |
| 7 | chr2:67728600-67730800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 8 | chr2:67728800-67729200 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 9 | chr2:67728800-67729800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
