Variant report

Variant rs145042370
Chromosome Location chr19:43771410-43771411
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43767200-43772000 Enhancers NHDF-Ad bronchial
2 chr19:43768000-43771600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr19:43768000-43771600 Enhancers HMEC breast
4 chr19:43768200-43771600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr19:43768200-43771600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr19:43768200-43771600 Enhancers Osteobl bone
7 chr19:43768200-43772000 Enhancers Hela-S3 cervix
8 chr19:43768200-43772200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr19:43769000-43771600 Enhancers NHLF lung
10 chr19:43770200-43772000 Enhancers NHEK skin
11 chr19:43770400-43773200 Active TSS Placenta Placenta
12 chr19:43770800-43772000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr19:43771200-43771600 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
14 chr19:43771400-43773400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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