Variant report

Variant rs73033960
Chromosome Location chr5:2008831-2008832
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:2007400-2011800 Enhancers Fetal Heart heart
2 chr5:2007800-2009400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
3 chr5:2008400-2009000 Bivalent Enhancer Fetal Lung lung
4 chr5:2008400-2009600 Bivalent Enhancer Fetal Stomach stomach
5 chr5:2008600-2009000 Enhancers Adipose Nuclei Adipose
6 chr5:2008600-2009000 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
7 chr5:2008600-2009000 Enhancers HMEC breast
8 chr5:2008600-2009200 Weak transcription Left Ventricle heart
9 chr5:2008600-2009400 Enhancers Right Ventricle heart
10 chr5:2008600-2009600 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr5:2008600-2012000 Weak transcription Right Atrium heart
12 chr5:2008800-2009000 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr5:2008800-2009000 Enhancers NHEK skin
14 chr5:2008800-2009200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr5:2008800-2009400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr5:2008800-2009400 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr5:2008800-2010200 Bivalent Enhancer Fetal Muscle Leg muscle
18 chr5:2008800-2010400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
19 chr5:2008800-2011600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr5:2008800-2013200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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