Variant report

Variant rs1811754
Chromosome Location chr4:189330185-189330186
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:189328000-189331800 Enhancers NHDF-Ad bronchial
2 chr4:189328400-189330200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr4:189328400-189331800 Enhancers Fetal Intestine Small intestine
4 chr4:189328800-189330200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr4:189328800-189330400 Enhancers Fetal Heart heart
6 chr4:189329000-189330200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr4:189329000-189330200 Enhancers Placenta Amnion Placenta Amnion
8 chr4:189329000-189330200 Enhancers HMEC breast
9 chr4:189329000-189330400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr4:189329200-189330200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr4:189329400-189330800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr4:189329600-189330400 Enhancers Osteobl bone
13 chr4:189330000-189330400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
14 chr4:189330000-189330600 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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