Variant report
Variant | rs567241727 |
---|---|
Chromosome Location | chr2:185550454-185550455 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:185544200-185550600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr2:185545200-185557000 | Weak transcription | Fetal Stomach | stomach |
3 | chr2:185545800-185552200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr2:185546000-185550600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr2:185548600-185552200 | Enhancers | NHEK | skin |
6 | chr2:185549000-185551000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
7 | chr2:185549200-185550600 | Weak transcription | HMEC | breast |
8 | chr2:185550000-185550800 | ZNF genes & repeats | Foreskin Fibroblast Primary Cells skin02 | Skin |
9 | chr2:185550200-185552000 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
10 | chr2:185550400-185551200 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |