Variant report

Variant rs8108042
Chromosome Location chr19:43389203-43389204
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43386200-43389400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr19:43387600-43390600 Weak transcription NHEK skin
3 chr19:43387800-43391600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr19:43388400-43389400 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr19:43388600-43389400 Enhancers Placenta Placenta
6 chr19:43388600-43389600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr19:43388600-43389600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr19:43388600-43389600 Enhancers A549 lung
9 chr19:43388600-43389800 Enhancers HSMMtube muscle
10 chr19:43388800-43389400 Enhancers HMEC breast
11 chr19:43388800-43389600 Enhancers Muscle Satellite Cultured Cells --
12 chr19:43388800-43389800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr19:43389000-43389600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr19:43389000-43389600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr19:43389000-43389600 Enhancers NHDF-Ad bronchial
16 chr19:43389200-43389400 Enhancers HSMM muscle
17 chr19:43389200-43389400 Weak transcription NHLF lung
18 chr19:43389200-43391800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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