Variant report

Variant rs1694042
Chromosome Location chr3:21996348-21996349
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:21995800-21996800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr3:21995800-21997400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr3:21995800-21997800 Enhancers Liver Liver
4 chr3:21996000-21996400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr3:21996000-21997000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr3:21996000-21997000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr3:21996000-21997200 Enhancers Muscle Satellite Cultured Cells --

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