Variant report

Variant rs34804863
Chromosome Location chr12:1626043-1626044
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:1614200-1626200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:1619600-1626400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr12:1624200-1626600 Weak transcription HSMM muscle
4 chr12:1625600-1626400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr12:1625800-1626400 Enhancers NHEK skin
6 chr12:1626000-1626400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr12:1626000-1626400 Enhancers HMEC breast
8 chr12:1626000-1626600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr12:1626000-1627400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr12:1626000-1628000 Enhancers Muscle Satellite Cultured Cells --
11 chr12:1626000-1629400 Enhancers NHDF-Ad bronchial

Quick Search:


  
Input of quick search could be:

what's new

Quick links