Variant report
Variant | rs11623477 |
---|---|
Chromosome Location | chr14:71715883-71715884 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:71709600-71717800 | Weak transcription | Fetal Lung | lung |
2 | chr14:71714000-71717200 | Weak transcription | Primary T cells from cord blood | blood |
3 | chr14:71714200-71716600 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr14:71714200-71716800 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
5 | chr14:71715400-71719600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr14:71715600-71717200 | Weak transcription | Osteobl | bone |
7 | chr14:71715600-71729000 | Weak transcription | Fetal Heart | heart |
8 | chr14:71715800-71716800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |