Variant report
| Variant | rs73974713 |
|---|---|
| Chromosome Location | chr2:181892948-181892949 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:181856800-181897200 | Weak transcription | Primary B cells from cord blood | blood |
| 2 | chr2:181857800-181901200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 3 | chr2:181860000-181894800 | Weak transcription | Primary hematopoietic stem cells | blood |
| 4 | chr2:181873400-181901000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr2:181886000-181901200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 6 | chr2:181890200-181895600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 7 | chr2:181890800-181901200 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
