Variant report

Variant rs7035786
Chromosome Location chr9:94920743-94920744
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:94910200-94923800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr9:94911200-94925600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:94916400-94931800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:94917600-94922800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr9:94920400-94920800 Enhancers Placenta Placenta
6 chr9:94920400-94921200 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:94920400-94921200 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
8 chr9:94920600-94920800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr9:94920600-94920800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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