Variant report

Variant rs56384623
Chromosome Location chr19:43704942-43704943
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43691000-43705000 Weak transcription NHLF lung
2 chr19:43692200-43705000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr19:43704000-43708200 Enhancers HMEC breast
4 chr19:43704200-43706000 Enhancers NHEK skin
5 chr19:43704200-43706600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr19:43704200-43708200 Enhancers Osteobl bone
7 chr19:43704400-43706800 Enhancers NH-A brain
8 chr19:43704400-43707400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr19:43704400-43707400 Enhancers NHDF-Ad bronchial
10 chr19:43704600-43705000 Active TSS Placenta Placenta
11 chr19:43704800-43706000 Enhancers Liver Liver
12 chr19:43704800-43707800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr19:43704800-43708000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr19:43704800-43708800 Enhancers Muscle Satellite Cultured Cells --

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