Variant report

Variant rs73025714
Chromosome Location chr2:168033646-168033647
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168016200-168034200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:168032600-168037600 Weak transcription Gastric stomach
3 chr2:168033200-168033800 Enhancers HSMM muscle
4 chr2:168033200-168035400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:168033400-168033800 Flanking Active TSS Muscle Satellite Cultured Cells --
6 chr2:168033400-168034000 Enhancers NHDF-Ad bronchial
7 chr2:168033400-168034200 Enhancers Osteobl bone
8 chr2:168033400-168034400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr2:168033400-168035000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr2:168033400-168035400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:168033600-168034600 Weak transcription NHLF lung

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