Variant report

Variant rs8109810
Chromosome Location chr19:43770253-43770254
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43767200-43772000 Enhancers NHDF-Ad bronchial
2 chr19:43767800-43770400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
3 chr19:43768000-43771600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr19:43768000-43771600 Enhancers HMEC breast
5 chr19:43768200-43771200 Enhancers NH-A brain
6 chr19:43768200-43771400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr19:43768200-43771600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr19:43768200-43771600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr19:43768200-43771600 Enhancers Osteobl bone
10 chr19:43768200-43772000 Enhancers Hela-S3 cervix
11 chr19:43768200-43772200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr19:43768800-43771400 Enhancers Muscle Satellite Cultured Cells --
13 chr19:43769000-43770400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr19:43769000-43771600 Enhancers NHLF lung
15 chr19:43769400-43770600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr19:43770000-43770400 Flanking Active TSS Placenta Placenta
17 chr19:43770000-43770800 Active TSS Breast Myoepithelial Primary Cells Breast
18 chr19:43770200-43770600 Weak transcription A549 lung
19 chr19:43770200-43772000 Enhancers NHEK skin

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