Variant report

Variant rs11788585
Chromosome Location chr9:93678677-93678678
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93658800-93683400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:93674000-93681800 Weak transcription Pancreas Pancrea
3 chr9:93677000-93679200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr9:93677400-93681600 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr9:93677400-93682000 Weak transcription Fetal Muscle Leg muscle
6 chr9:93677400-93682200 Weak transcription Fetal Brain Male brain
7 chr9:93677600-93679600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr9:93677800-93678800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:93677800-93681400 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr9:93677800-93682200 Weak transcription Fetal Heart heart
11 chr9:93677800-93682400 Weak transcription HMEC breast
12 chr9:93678000-93680600 Weak transcription Stomach Mucosa stomach
13 chr9:93678000-93681400 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr9:93678400-93679200 Enhancers NHDF-Ad bronchial
15 chr9:93678600-93678800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr9:93678600-93679200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr9:93678600-93683200 Weak transcription Liver Liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links