Variant report

Variant rs62335359
Chromosome Location chr4:158964341-158964342
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:158959200-158965600 Weak transcription Pancreas Pancrea
2 chr4:158962000-158964800 Enhancers HSMMtube muscle
3 chr4:158962600-158964600 Enhancers HSMM muscle
4 chr4:158963400-158964400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:158963400-158964400 Enhancers HMEC breast
6 chr4:158963400-158964600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr4:158963400-158964600 Enhancers HUVEC blood vessel
8 chr4:158963400-158964600 Enhancers NH-A brain
9 chr4:158963400-158965400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr4:158963600-158964400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr4:158963800-158964400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr4:158964000-158964600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr4:158964000-158964800 Enhancers Osteobl bone
14 chr4:158964200-158964400 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr4:158964200-158964400 Flanking Active TSS Muscle Satellite Cultured Cells --
16 chr4:158964200-158964400 Flanking Active TSS NHDF-Ad bronchial
17 chr4:158964200-158964600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr4:158964200-158964600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin

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