Variant report

Variant rs371735336
Chromosome Location chr16:12671499-12671500
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:12652600-12672200 Weak transcription Right Ventricle heart
2 chr16:12662800-12672000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr16:12668400-12672400 Weak transcription Fetal Intestine Small intestine
4 chr16:12668600-12672200 Enhancers Primary B cells from peripheral blood blood
5 chr16:12669400-12673000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr16:12670200-12672000 Enhancers Primary B cells from cord blood blood
7 chr16:12670800-12674400 Weak transcription GM12878-XiMat blood
8 chr16:12671000-12678400 Weak transcription Gastric stomach
9 chr16:12671200-12672000 Enhancers Fetal Brain Male brain
10 chr16:12671200-12677600 Weak transcription HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links