Variant report

Variant rs28493914
Chromosome Location chr19:43388802-43388803
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43382200-43389000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr19:43384000-43389000 Weak transcription NHDF-Ad bronchial
3 chr19:43384400-43389000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr19:43386200-43389400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr19:43387600-43390600 Weak transcription NHEK skin
6 chr19:43387800-43391600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr19:43388400-43389400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr19:43388600-43389400 Enhancers Placenta Placenta
9 chr19:43388600-43389600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr19:43388600-43389600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr19:43388600-43389600 Enhancers A549 lung
12 chr19:43388600-43389800 Enhancers HSMMtube muscle
13 chr19:43388800-43389400 Enhancers HMEC breast
14 chr19:43388800-43389600 Enhancers Muscle Satellite Cultured Cells --
15 chr19:43388800-43389800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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