Variant report
| Variant | rs16953933 |
|---|---|
| Chromosome Location | chr13:97855566-97855567 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:97846400-97858200 | Weak transcription | Fetal Intestine Small | intestine |
| 2 | chr13:97847400-97858200 | Weak transcription | HSMM | muscle |
| 3 | chr13:97849400-97855800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr13:97850600-97857000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 5 | chr13:97852600-97856400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 6 | chr13:97852600-97858200 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 7 | chr13:97853400-97857800 | Weak transcription | HUVEC | blood vessel |
| 8 | chr13:97853400-97861600 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
