Variant report
| Variant | rs56844899 |
|---|---|
| Chromosome Location | chr3:157039518-157039519 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:157015600-157048400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr3:157030600-157047000 | Weak transcription | Osteobl | bone |
| 3 | chr3:157036000-157047800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 4 | chr3:157036200-157040400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 5 | chr3:157036800-157053000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 6 | chr3:157039200-157039600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 7 | chr3:157039200-157039800 | Enhancers | HUVEC | blood vessel |
