Variant report
Variant | rs17127998 |
---|---|
Chromosome Location | chr14:55303076-55303077 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:55293800-55306400 | Weak transcription | Aorta | Aorta |
2 | chr14:55299200-55308200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr14:55300400-55305800 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr14:55301000-55305600 | Enhancers | Liver | Liver |
5 | chr14:55301000-55305800 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
6 | chr14:55301000-55310000 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
7 | chr14:55301800-55306000 | Enhancers | HepG2 | liver |
8 | chr14:55301800-55306400 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
9 | chr14:55302200-55303200 | Weak transcription | Fetal Intestine Small | intestine |
10 | chr14:55302800-55303600 | Enhancers | Fetal Intestine Large | intestine |