Variant report
| Variant | rs73124222 |
|---|---|
| Chromosome Location | chr1:223529390-223529391 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:223514400-223535800 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 2 | chr1:223526600-223530200 | Weak transcription | Esophagus | oesophagus |
| 3 | chr1:223526600-223534000 | Weak transcription | Primary T cells from cord blood | blood |
| 4 | chr1:223528000-223535000 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
| 5 | chr1:223528000-223536400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 6 | chr1:223528200-223529800 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr1:223528200-223530000 | Enhancers | NHEK | skin |
| 8 | chr1:223528600-223530600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr1:223528600-223530600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 10 | chr1:223528800-223529400 | Enhancers | HMEC | breast |
