Variant report

Variant rs12002641
Chromosome Location chr9:117573803-117573804
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117568800-117576200 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr9:117569800-117582600 Weak transcription Pancreas Pancrea
3 chr9:117572800-117576200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr9:117573200-117577600 Weak transcription H9 Cell Line embryonic stem cell
5 chr9:117573400-117574600 Enhancers HMEC breast
6 chr9:117573600-117574000 Enhancers Brain Hippocampus Middle brain
7 chr9:117573600-117574600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr9:117573600-117575400 Enhancers Placenta Amnion Placenta Amnion
9 chr9:117573600-117575600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:117573600-117576200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr9:117573800-117574000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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