Variant report
Variant | rs12229912 |
---|---|
Chromosome Location | chr12:56049276-56049277 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:56045400-56050200 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
2 | chr12:56045800-56050800 | Weak transcription | HepG2 | liver |
3 | chr12:56046400-56050200 | Weak transcription | Duodenum Mucosa | Duodenum |
4 | chr12:56046600-56050200 | Weak transcription | Primary B cells from peripheral blood | blood |
5 | chr12:56047000-56049800 | Weak transcription | Fetal Intestine Small | intestine |
6 | chr12:56047000-56050000 | Weak transcription | Fetal Intestine Large | intestine |
7 | chr12:56048400-56049400 | Enhancers | Fetal Muscle Leg | muscle |
8 | chr12:56048600-56050400 | Enhancers | Fetal Muscle Trunk | muscle |
9 | chr12:56049000-56051400 | Weak transcription | Lung | lung |
10 | chr12:56049000-56052600 | Weak transcription | HSMM | muscle |
11 | chr12:56049200-56050200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |