Variant report
| Variant | rs6918767 |
|---|---|
| Chromosome Location | chr6:139707585-139707586 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:139700600-139709400 | Weak transcription | Fetal Intestine Large | intestine |
| 2 | chr6:139700600-139713800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 3 | chr6:139701400-139707600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 4 | chr6:139703000-139707600 | Weak transcription | K562 | blood |
| 5 | chr6:139705800-139707600 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 6 | chr6:139706200-139713800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
| 7 | chr6:139706400-139707600 | Weak transcription | HepG2 | liver |
| 8 | chr6:139706400-139713800 | Weak transcription | Osteobl | bone |
| 9 | chr6:139707400-139708000 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
| 10 | chr6:139707400-139708200 | Enhancers | Placenta Amnion | Placenta Amnion |
