Variant report

Variant rs10423386
Chromosome Location chr19:43392025-43392026
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43390600-43393200 Enhancers NHEK skin
2 chr19:43391200-43392200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr19:43391200-43395400 Enhancers HMEC breast
4 chr19:43391400-43392200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr19:43391400-43392200 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr19:43391400-43392200 Enhancers NHDF-Ad bronchial
7 chr19:43391600-43392200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr19:43391600-43392600 Enhancers Muscle Satellite Cultured Cells --
9 chr19:43391600-43393400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr19:43391800-43392200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr19:43391800-43392200 Enhancers NH-A brain
12 chr19:43391800-43392200 Enhancers NHLF lung
13 chr19:43392000-43393000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr19:43392000-43393200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr19:43392000-43394800 Weak transcription Placenta Placenta

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