Variant report

Variant rs73171446
Chromosome Location chr13:39722620-39722621
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:39719800-39722800 Weak transcription Adipose Nuclei Adipose
2 chr13:39722400-39723400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr13:39722400-39723400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr13:39722400-39723400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr13:39722400-39723400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr13:39722400-39723400 Bivalent Enhancer NHDF-Ad bronchial
7 chr13:39722400-39723600 Enhancers HMEC breast
8 chr13:39722400-39723600 Enhancers NHEK skin
9 chr13:39722600-39722800 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr13:39722600-39722800 Flanking Active TSS GM12878-XiMat blood
11 chr13:39722600-39723200 Active TSS Pancreatic Islets Pancreatic Islet
12 chr13:39722600-39723200 Enhancers Ovary ovary
13 chr13:39722600-39723200 Enhancers NHLF lung
14 chr13:39722600-39724400 Enhancers ES-I3 Cell Line embryonic stem cell

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