Variant report

Variant rs568160622
Chromosome Location chr9:116839266-116839267
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116834600-116839800 Weak transcription Fetal Intestine Small intestine
2 chr9:116834800-116839600 Weak transcription Gastric stomach
3 chr9:116835400-116840200 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr9:116837200-116842400 Enhancers A549 lung
5 chr9:116838800-116840600 Active TSS Liver Liver
6 chr9:116838800-116840600 Bivalent/Poised TSS HepG2 liver
7 chr9:116839000-116839800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr9:116839000-116841600 Enhancers Rectal Mucosa Donor 31 rectum
9 chr9:116839000-116845200 Enhancers Stomach Mucosa stomach
10 chr9:116839200-116839800 Active TSS Pancreas Pancrea
11 chr9:116839200-116840600 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links