Variant report

Variant rs72913594
Chromosome Location chr1:59293000-59293001
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59282400-59293800 Weak transcription Aorta Aorta
2 chr1:59283200-59293600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr1:59290400-59293800 Weak transcription Gastric stomach
4 chr1:59291000-59293800 Weak transcription Left Ventricle heart
5 chr1:59291000-59295800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:59291000-59296200 Weak transcription Ovary ovary
7 chr1:59291000-59298400 Weak transcription Placenta Amnion Placenta Amnion
8 chr1:59291600-59293200 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:59292000-59294400 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:59292400-59294000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr1:59292800-59294400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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