Variant report

Variant rs28526801
Chromosome Location chr19:43388667-43388668
allele A/C
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 chr19:43387600-43388800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr19:43387600-43388800 Weak transcription HMEC breast
7 chr19:43387600-43390600 Weak transcription NHEK skin
8 chr19:43387800-43388800 Weak transcription Muscle Satellite Cultured Cells --
9 chr19:43387800-43391600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr19:43388400-43389400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr19:43388600-43389400 Enhancers Placenta Placenta
12 chr19:43388600-43389600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr19:43388600-43389600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr19:43388600-43389600 Enhancers A549 lung
15 chr19:43388600-43389800 Enhancers HSMMtube muscle

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