Variant report

Variant rs28664906
Chromosome Location chr19:43385862-43385863
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43381600-43386000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr19:43381600-43386200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr19:43381600-43386200 Weak transcription NHEK skin
4 chr19:43381600-43387000 Weak transcription Muscle Satellite Cultured Cells --
5 chr19:43382200-43389000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr19:43384000-43389000 Weak transcription NHDF-Ad bronchial
7 chr19:43384400-43386200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr19:43384400-43388400 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr19:43384400-43389000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr19:43385600-43387600 Enhancers HMEC breast
11 chr19:43385600-43388600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr19:43385600-43388600 Weak transcription Placenta Placenta

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