Variant report
| Variant | rs61770442 |
|---|---|
| Chromosome Location | chr1:85263580-85263581 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:85241000-85263600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr1:85263000-85263600 | Enhancers | Esophagus | oesophagus |
| 3 | chr1:85263000-85264000 | Enhancers | Left Ventricle | heart |
| 4 | chr1:85263200-85263600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 5 | chr1:85263200-85263600 | Enhancers | HMEC | breast |
| 6 | chr1:85263200-85264000 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr1:85263200-85264000 | Enhancers | NHEK | skin |
| 8 | chr1:85263200-85264600 | Enhancers | Fetal Heart | heart |
| 9 | chr1:85263400-85264000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
