Variant report

Variant rs62141166
Chromosome Location chr2:31669516-31669517
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31653400-31669600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:31668400-31669600 Enhancers Fetal Intestine Small intestine
3 chr2:31669000-31670400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr2:31669000-31670800 Enhancers NHDF-Ad bronchial
5 chr2:31669200-31670600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr2:31669200-31670600 Enhancers Muscle Satellite Cultured Cells --
7 chr2:31669200-31670600 Enhancers Osteobl bone
8 chr2:31669200-31670800 Enhancers HSMM muscle
9 chr2:31669400-31669800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:31669400-31670400 Enhancers HSMMtube muscle
11 chr2:31669400-31670800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr2:31669400-31671200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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