Variant report
| Variant | rs4650681 |
|---|---|
| Chromosome Location | chr1:185411855-185411856 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:185407000-185412000 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |
| 2 | chr1:185407400-185412200 | Weak transcription | Right Atrium | heart |
| 3 | chr1:185408200-185412000 | Enhancers | Primary T cells fromperipheralblood | blood |
| 4 | chr1:185409000-185412000 | Enhancers | Fetal Heart | heart |
| 5 | chr1:185410200-185412400 | Enhancers | Fetal Kidney | kidney |
| 6 | chr1:185411400-185412000 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 7 | chr1:185411600-185412200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 8 | chr1:185411600-185420200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr1:185411800-185416400 | Weak transcription | A549 | lung |
