Variant report

Variant rs10037038
Chromosome Location chr5:112681165-112681166
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112667200-112693400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:112678800-112681400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr5:112678800-112681600 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr5:112678800-112682400 Enhancers HMEC breast
5 chr5:112679000-112682000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:112679400-112681400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr5:112679800-112683000 Weak transcription Fetal Stomach stomach
8 chr5:112680400-112682000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr5:112680600-112682000 Enhancers NHEK skin
10 chr5:112680800-112681200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr5:112680800-112681200 Enhancers Fetal Heart heart
12 chr5:112681000-112681200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr5:112681000-112681200 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
14 chr5:112681000-112681200 Enhancers Pancreas Pancrea
15 chr5:112681000-112681200 Enhancers Right Ventricle heart
16 chr5:112681000-112681400 Enhancers Esophagus oesophagus
17 chr5:112681000-112681600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr5:112681000-112681800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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