Variant report
Variant | rs9495462 |
---|---|
Chromosome Location | chr6:139707704-139707705 |
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 | chr6:139706200-139713800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
4 | chr6:139706400-139713800 | Weak transcription | Osteobl | bone |
5 | chr6:139707400-139708000 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
6 | chr6:139707400-139708200 | Enhancers | Placenta Amnion | Placenta Amnion |
7 | chr6:139707600-139708000 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
8 | chr6:139707600-139708000 | Enhancers | Skeletal Muscle Female | skeletal muscle |
9 | chr6:139707600-139708000 | Enhancers | HepG2 | liver |
10 | chr6:139707600-139708000 | Enhancers | K562 | blood |
11 | chr6:139707600-139708400 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |