Variant report
Variant | rs9869929 |
---|---|
Chromosome Location | chr3:69879355-69879356 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:69869200-69879400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr3:69869200-69879400 | Weak transcription | Pancreas | Pancrea |
3 | chr3:69870200-69886000 | Weak transcription | Aorta | Aorta |
4 | chr3:69870600-69886200 | Weak transcription | Colon Smooth Muscle | Colon |
5 | chr3:69873800-69887600 | Weak transcription | NHLF | lung |
6 | chr3:69874000-69881000 | Weak transcription | Ovary | ovary |
7 | chr3:69876400-69881200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr3:69878200-69879600 | Enhancers | Skeletal Muscle Female | skeletal muscle |
9 | chr3:69879000-69879600 | Enhancers | Left Ventricle | heart |
10 | chr3:69879000-69879600 | Enhancers | Psoas Muscle | Psoas |
11 | chr3:69879000-69879600 | Enhancers | Right Atrium | heart |
12 | chr3:69879000-69879600 | Enhancers | Right Ventricle | heart |
13 | chr3:69879200-69879400 | Enhancers | Fetal Heart | heart |
14 | chr3:69879200-69879600 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |