Variant report
| Variant | rs10495553 |
|---|---|
| Chromosome Location | chr2:7405900-7405901 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:7400200-7410000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr2:7400200-7428600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 3 | chr2:7404000-7414200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 4 | chr2:7404800-7406600 | Enhancers | Fetal Brain Male | brain |
| 5 | chr2:7405400-7410200 | Weak transcription | Fetal Brain Female | brain |
