Variant report

Variant rs28447290
Chromosome Location chr19:43435152-43435153
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr19:43425800-43435400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr19:43427600-43435800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr19:43433800-43439600 Enhancers HMEC breast
6 chr19:43434000-43435400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr19:43434200-43435800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr19:43434200-43440200 Enhancers NHDF-Ad bronchial
9 chr19:43434400-43435400 Weak transcription Placenta Placenta
10 chr19:43434600-43437000 Enhancers NHLF lung
11 chr19:43434800-43435800 Weak transcription Osteobl bone
12 chr19:43434800-43439800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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