Variant report

Variant rs372011857
Chromosome Location chr9:110651789-110651790
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110635800-110656800 Weak transcription H9 Cell Line embryonic stem cell
2 chr9:110644800-110658800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:110646800-110652600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:110649200-110657000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr9:110650600-110652200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:110650800-110651800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr9:110650800-110651800 Enhancers Adipose Nuclei Adipose
8 chr9:110651000-110651800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr9:110651000-110651800 Enhancers Ovary ovary
10 chr9:110651000-110652000 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr9:110651000-110652200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr9:110651000-110652200 Enhancers Skeletal Muscle Female skeletal muscle
13 chr9:110651400-110653200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr9:110651600-110656800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr9:110651600-110656800 Weak transcription Right Atrium heart

Quick Search:


  
Input of quick search could be:

what's new

Quick links