Variant report
Variant | rs10096185 |
---|---|
Chromosome Location | chr8:50022640-50022641 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:50019000-50023400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
2 | chr8:50019200-50023600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
3 | chr8:50020600-50025800 | Weak transcription | Fetal Lung | lung |
4 | chr8:50022200-50023600 | Enhancers | NHEK | skin |
5 | chr8:50022400-50023200 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
6 | chr8:50022400-50023200 | Enhancers | Pancreas | Pancrea |
7 | chr8:50022400-50023400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr8:50022400-50023400 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
9 | chr8:50022400-50023400 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
10 | chr8:50022400-50023400 | Enhancers | HMEC | breast |
11 | chr8:50022600-50023000 | Weak transcription | Stomach Mucosa | stomach |
12 | chr8:50022600-50023400 | Weak transcription | Gastric | stomach |
13 | chr8:50022600-50023600 | Enhancers | K562 | blood |