Variant report
| Variant | rs4764952 |
|---|---|
| Chromosome Location | chr12:103723239-103723240 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:103707200-103786400 | Weak transcription | Primary B cells from cord blood | blood |
| 2 | chr12:103712600-103734800 | Weak transcription | Primary B cells from peripheral blood | blood |
| 3 | chr12:103722200-103725800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 4 | chr12:103723000-103725800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 5 | chr12:103723200-103727600 | Weak transcription | Fetal Brain Male | brain |
