Variant report
Variant | rs59509049 |
---|---|
Chromosome Location | chr2:190988968-190988969 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:190985000-190997200 | Weak transcription | Left Ventricle | heart |
2 | chr2:190988200-190989400 | Enhancers | Placenta | Placenta |
3 | chr2:190988400-190989000 | Enhancers | NH-A | brain |
4 | chr2:190988400-190989200 | Enhancers | NHDF-Ad | bronchial |
5 | chr2:190988400-190989200 | Enhancers | Osteobl | bone |
6 | chr2:190988400-190989400 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
7 | chr2:190988400-190990000 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
8 | chr2:190988600-190989000 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
9 | chr2:190988800-190989000 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
10 | chr2:190988800-190989400 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
11 | chr2:190988800-190989400 | Enhancers | Fetal Intestine Large | intestine |