Variant report

Variant rs9427064
Chromosome Location chr1:161451639-161451640
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:161450200-161452600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:161450200-161452600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:161450200-161452600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:161450200-161452600 Enhancers HMEC breast
5 chr1:161450400-161452000 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
6 chr1:161450400-161452600 Enhancers NHEK skin
7 chr1:161450600-161452000 Enhancers Esophagus oesophagus
8 chr1:161450600-161458400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:161451000-161455000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr1:161451600-161451800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
11 chr1:161451600-161451800 Bivalent Enhancer Primary mononuclear cells fromperipheralblood Blood
12 chr1:161451600-161451800 Bivalent Enhancer Right Ventricle heart
13 chr1:161451600-161452600 Weak transcription K562 blood

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