Variant report

Variant rs190181086
Chromosome Location chr2:40166385-40166386
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40147000-40167400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:40164600-40166400 Flanking Active TSS Dnd41 blood
3 chr2:40164800-40166400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:40164800-40166400 Enhancers HSMM muscle
5 chr2:40164800-40166400 Enhancers Osteobl bone
6 chr2:40165000-40166400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:40165000-40166600 Enhancers Muscle Satellite Cultured Cells --
8 chr2:40165000-40166600 Enhancers NH-A brain
9 chr2:40165000-40166800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr2:40165000-40175800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr2:40165200-40166400 Enhancers HUES64 Cell Line embryonic stem cell
12 chr2:40165200-40166400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr2:40165400-40166400 Enhancers HMEC breast
14 chr2:40165600-40169400 Weak transcription HSMMtube muscle
15 chr2:40165600-40175200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links