Variant report
Variant | rs370354514 |
---|---|
Chromosome Location | chr8:124854707-124854708 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:124850800-124855200 | Weak transcription | Aorta | Aorta |
2 | chr8:124852200-124855200 | Weak transcription | Duodenum Mucosa | Duodenum |
3 | chr8:124852800-124856800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
4 | chr8:124853000-124856600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
5 | chr8:124853400-124854800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr8:124853400-124856600 | Weak transcription | NHEK | skin |
7 | chr8:124853600-124856600 | Weak transcription | HMEC | breast |
8 | chr8:124853800-124855000 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
9 | chr8:124854200-124856000 | ZNF genes & repeats | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |