Variant report

Variant rs11833064
Chromosome Location chr12:56768638-56768639
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
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

Quick Search:


  
Input of quick search could be:

what's new

Quick links