Variant report

Variant rs73016707
Chromosome Location chr1:152733090-152733091
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:152726800-152734200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr1:152729000-152735000 Enhancers HMEC breast
3 chr1:152729200-152735000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:152730600-152734200 Weak transcription NHLF lung
5 chr1:152730600-152734600 Enhancers Esophagus oesophagus
6 chr1:152731800-152734200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
7 chr1:152732000-152733400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr1:152732000-152733600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:152732000-152734800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:152732800-152734800 Enhancers NHEK skin
11 chr1:152733000-152734000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:152733000-152734400 Enhancers Placenta Placenta

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