Variant report

Variant rs12976627
Chromosome Location chr19:43687005-43687006
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43684000-43688400 Enhancers HMEC breast
2 chr19:43685200-43688000 Enhancers Hela-S3 cervix
3 chr19:43685200-43688200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr19:43685200-43688200 Enhancers Muscle Satellite Cultured Cells --
5 chr19:43685200-43691000 Enhancers Osteobl bone
6 chr19:43685400-43687400 Enhancers NHDF-Ad bronchial
7 chr19:43686200-43690400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr19:43686400-43687200 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr19:43686400-43687200 Weak transcription Placenta Placenta
10 chr19:43686400-43687400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr19:43686400-43688400 Enhancers NHEK skin
12 chr19:43686800-43687200 Weak transcription A549 lung
13 chr19:43686800-43687200 Weak transcription NHLF lung
14 chr19:43687000-43687400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr19:43687000-43688400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr19:43687000-43688400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr19:43687000-43688400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr19:43687000-43689400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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