Variant report

Variant rs368660329
Chromosome Location chr9:116839721-116839722
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116834600-116839800 Weak transcription Fetal Intestine Small intestine
2 chr9:116835400-116840200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr9:116837200-116842400 Enhancers A549 lung
4 chr9:116838800-116840600 Active TSS Liver Liver
5 chr9:116838800-116840600 Bivalent/Poised TSS HepG2 liver
6 chr9:116839000-116839800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr9:116839000-116841600 Enhancers Rectal Mucosa Donor 31 rectum
8 chr9:116839000-116845200 Enhancers Stomach Mucosa stomach
9 chr9:116839200-116839800 Active TSS Pancreas Pancrea
10 chr9:116839200-116840600 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr9:116839400-116840800 Enhancers Fetal Lung lung
12 chr9:116839600-116841200 Enhancers Gastric stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links