Variant report

Variant rs28704748
Chromosome Location chr19:43435966-43435967
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43424000-43436400 Weak transcription Pancreas Pancrea
2 chr19:43433800-43439600 Enhancers HMEC breast
3 chr19:43434200-43440200 Enhancers NHDF-Ad bronchial
4 chr19:43434600-43437000 Enhancers NHLF lung
5 chr19:43434800-43439800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr19:43435400-43436400 Enhancers Placenta Placenta
7 chr19:43435400-43436600 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr19:43435400-43439600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr19:43435600-43436600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr19:43435800-43436000 Enhancers A549 lung
11 chr19:43435800-43437000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr19:43435800-43438400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr19:43435800-43438600 Enhancers NHEK skin
14 chr19:43435800-43439200 Enhancers Osteobl bone
15 chr19:43435800-43439400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr19:43435800-43439600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr19:43435800-43439800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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