Variant report
| Variant | rs1200002 |
|---|---|
| Chromosome Location | chr13:37700488-37700489 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:37683800-37701400 | Weak transcription | Gastric | stomach |
| 2 | chr13:37694200-37700800 | Weak transcription | Fetal Heart | heart |
| 3 | chr13:37695600-37702600 | Weak transcription | Right Atrium | heart |
| 4 | chr13:37699000-37701000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 5 | chr13:37700200-37701000 | Enhancers | Fetal Lung | lung |
| 6 | chr13:37700200-37701000 | Enhancers | HUVEC | blood vessel |
| 7 | chr13:37700400-37702400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
