The 2.0 version of rSNPBase

Variant report

Variant rs10408171
Chromosome Location chr19:43388591-43388592
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr19:43385600-43388600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr19:43385600-43388600 Weak transcription Placenta Placenta
6 chr19:43386200-43389400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr19:43387600-43388800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr19:43387600-43388800 Weak transcription HMEC breast
9 chr19:43387600-43390600 Weak transcription NHEK skin
10 chr19:43387800-43388800 Weak transcription Muscle Satellite Cultured Cells --
11 chr19:43387800-43391600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr19:43388200-43388600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr19:43388400-43389400 Enhancers Breast Myoepithelial Primary Cells Breast

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Last update: Aug 31, 2015