Variant report

Variant rs55843038
Chromosome Location chr19:43492034-43492035
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43490000-43492200 Weak transcription Osteobl bone
2 chr19:43490800-43494600 Enhancers NHEK skin
3 chr19:43491000-43492200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr19:43491000-43492200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr19:43491400-43492400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr19:43491600-43492600 Enhancers HMEC breast
7 chr19:43491600-43492600 Enhancers NHDF-Ad bronchial
8 chr19:43491800-43492200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr19:43491800-43492200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr19:43491800-43492200 Weak transcription Placenta Placenta
11 chr19:43491800-43492200 Enhancers Placenta Amnion Placenta Amnion
12 chr19:43491800-43492200 Enhancers NHLF lung
13 chr19:43491800-43492400 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr19:43492000-43492400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr19:43492000-43492400 Enhancers Muscle Satellite Cultured Cells --

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