Variant report

Variant rs370865094
Chromosome Location chr6:33496740-33496741
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33494600-33497400 Weak transcription HepG2 liver
2 chr6:33496200-33496800 Enhancers Fetal Stomach stomach
3 chr6:33496400-33496800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
4 chr6:33496400-33496800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
5 chr6:33496400-33496800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links