Variant report

Variant rs17662053
Chromosome Location chr18:29372270-29372271
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29363200-29375600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr18:29369600-29373600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr18:29369600-29375000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr18:29369600-29377200 Weak transcription H9 Cell Line embryonic stem cell
5 chr18:29370400-29372800 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr18:29371000-29372600 Enhancers Primary monocytes fromperipheralblood blood
7 chr18:29371000-29373000 Enhancers HepG2 liver
8 chr18:29371000-29373800 Enhancers Monocytes-CD14+_RO01746 blood
9 chr18:29371200-29373600 Enhancers Liver Liver
10 chr18:29371400-29372400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr18:29371400-29372600 Enhancers Primary Natural Killer cells fromperipheralblood blood
12 chr18:29372200-29372400 Enhancers GM12878-XiMat blood
13 chr18:29372200-29373400 Enhancers Fetal Intestine Small intestine
14 chr18:29372200-29373600 Enhancers Fetal Intestine Large intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links