Variant report
| Variant | rs6661346 |
|---|---|
| Chromosome Location | chr1:211859713-211859714 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:211855200-211860800 | Weak transcription | GM12878-XiMat | blood |
| 2 | chr1:211855400-211860800 | Weak transcription | Primary B cells from peripheral blood | blood |
| 3 | chr1:211855400-211861400 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
| 4 | chr1:211856400-211860600 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
| 5 | chr1:211859600-211859800 | Bivalent Enhancer | HepG2 | liver |
| 6 | chr1:211859600-211860800 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
| 7 | chr1:211859600-211868000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 8 | chr1:211859600-211872000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
