Variant report
| Variant | rs3904139 |
|---|---|
| Chromosome Location | chr13:97852388-97852389 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:97846200-97852400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 2 | chr13:97846400-97858200 | Weak transcription | Fetal Intestine Small | intestine |
| 3 | chr13:97847400-97858200 | Weak transcription | HSMM | muscle |
| 4 | chr13:97849400-97855800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 5 | chr13:97850000-97853000 | Weak transcription | HUVEC | blood vessel |
| 6 | chr13:97850600-97857000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 7 | chr13:97850800-97852600 | Enhancers | Placenta | Placenta |
| 8 | chr13:97851200-97852600 | Enhancers | Placenta Amnion | Placenta Amnion |
| 9 | chr13:97851200-97853600 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
| 10 | chr13:97852200-97853200 | Enhancers | Fetal Stomach | stomach |
