Variant report

Variant rs62277076
Chromosome Location chr3:156471143-156471144
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:156466800-156471200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
2 chr3:156469400-156471200 Enhancers HMEC breast
3 chr3:156469600-156471400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr3:156469800-156471200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr3:156470000-156471200 Enhancers Muscle Satellite Cultured Cells --
6 chr3:156470200-156471800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr3:156470200-156471800 Enhancers NHDF-Ad bronchial
8 chr3:156470200-156477800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr3:156470400-156471200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr3:156470800-156478000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:156471000-156471200 Enhancers H1 Cell Line embryonic stem cell
12 chr3:156471000-156471600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr3:156471000-156472000 Weak transcription Fetal Kidney kidney
14 chr3:156471000-156478400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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