Variant report
Variant | rs2228946 |
---|---|
Chromosome Location | chr7:116918085-116918086 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:116909600-116920400 | Weak transcription | Placenta Amnion | Placenta Amnion |
2 | chr7:116914600-116918200 | Weak transcription | Placenta | Placenta |
3 | chr7:116915000-116919600 | Strong transcription | Fetal Lung | lung |
4 | chr7:116915400-116918200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr7:116915400-116920000 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
6 | chr7:116915400-116920000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
7 | chr7:116915400-116920000 | Weak transcription | NHLF | lung |
8 | chr7:116915800-116920000 | Weak transcription | Right Atrium | heart |
9 | chr7:116917800-116919600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
10 | chr7:116918000-116918200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
11 | chr7:116918000-116921800 | Weak transcription | NHDF-Ad | bronchial |