Variant report
Variant | rs11833064 |
---|---|
Chromosome Location | chr12:56768638-56768639 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:56767400-56769000 | Enhancers | Primary B cells from cord blood | blood |
2 | chr12:56767400-56773600 | Enhancers | Primary B cells from peripheral blood | blood |
3 | chr12:56768000-56769200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
4 | chr12:56768200-56769400 | Enhancers | Fetal Intestine Small | intestine |
5 | chr12:56768200-56769800 | Enhancers | Monocytes-CD14+_RO01746 | blood |
6 | chr12:56768200-56771400 | Enhancers | Primary monocytes fromperipheralblood | blood |
7 | chr12:56768200-56771400 | Enhancers | HepG2 | liver |
8 | chr12:56768400-56769200 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |
9 | chr12:56768400-56770000 | Enhancers | Fetal Intestine Large | intestine |
10 | chr12:56768600-56769000 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
11 | chr12:56768600-56769200 | Enhancers | HUVEC | blood vessel |
12 | chr12:56768600-56770200 | Flanking Active TSS | GM12878-XiMat | blood |