Variant report
| Variant | rs12579358 |
|---|---|
| Chromosome Location | chr12:103719027-103719028 |
| allele | G/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 | chr12:103716800-103722200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 4 | chr12:103718800-103719200 | Enhancers | Fetal Brain Female | brain |
| 5 | chr12:103719000-103719600 | Enhancers | Brain Germinal Matrix | brain |
