Variant report

Variant rs2041108
Chromosome Location chr19:43435606-43435607
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43419400-43435800 Weak transcription NHEK skin
2 chr19:43424000-43436400 Weak transcription Pancreas Pancrea
3 chr19:43427600-43435800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr19:43433800-43439600 Enhancers HMEC breast
5 chr19:43434200-43435800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr19:43434200-43440200 Enhancers NHDF-Ad bronchial
7 chr19:43434600-43437000 Enhancers NHLF lung
8 chr19:43434800-43435800 Weak transcription Osteobl bone
9 chr19:43434800-43439800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr19:43435400-43436400 Enhancers Placenta Placenta
11 chr19:43435400-43436600 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr19:43435400-43439600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr19:43435600-43436600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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