Variant report

Variant rs71350644
Chromosome Location chr19:43688127-43688128
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43684000-43688400 Enhancers HMEC breast
2 chr19:43685200-43688200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr19:43685200-43688200 Enhancers Muscle Satellite Cultured Cells --
4 chr19:43685200-43691000 Enhancers Osteobl bone
5 chr19:43686200-43690400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr19:43686400-43688400 Enhancers NHEK skin
7 chr19:43687000-43688400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr19:43687000-43688400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr19:43687000-43688400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr19:43687000-43689400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr19:43687200-43690600 Active TSS Placenta Placenta
12 chr19:43687200-43691000 Enhancers NHLF lung
13 chr19:43687400-43688200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr19:43687800-43688400 Transcr. at gene 5' and 3' NHDF-Ad bronchial
15 chr19:43687800-43688600 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
16 chr19:43687800-43689000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links