Variant report

Variant rs10174725
Chromosome Location chr2:190222739-190222740
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190215800-190228400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:190216400-190225400 Weak transcription Muscle Satellite Cultured Cells --
3 chr2:190221800-190222800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr2:190221800-190222800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr2:190222000-190222800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr2:190222000-190227800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr2:190222200-190222800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr2:190222600-190222800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

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