Variant report

Variant rs4279297
Chromosome Location chr5:52698518-52698519
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:52694200-52698600 Weak transcription Fetal Heart heart
2 chr5:52694200-52702600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr5:52694400-52702800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr5:52696400-52698800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr5:52696400-52699000 Weak transcription NH-A brain
6 chr5:52696400-52699200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr5:52696400-52701600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr5:52696600-52699000 Weak transcription NHLF lung
9 chr5:52696600-52702200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr5:52697200-52702000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr5:52698200-52700400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr5:52698400-52698600 Enhancers HSMMtube muscle
13 chr5:52698400-52700400 Enhancers HSMM muscle
14 chr5:52698400-52700400 Enhancers Osteobl bone
15 chr5:52698400-52701600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr5:52698400-52704000 Enhancers NHDF-Ad bronchial

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