Variant report

Variant rs34942708
Chromosome Location chr5:52695974-52695975
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:52692400-52696400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr5:52692600-52697200 Enhancers NHDF-Ad bronchial
3 chr5:52692800-52696400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr5:52692800-52697200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr5:52693000-52696600 Enhancers NHLF lung
6 chr5:52693600-52696800 Enhancers Osteobl bone
7 chr5:52694200-52698600 Weak transcription Fetal Heart heart
8 chr5:52694200-52702600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr5:52694400-52696600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr5:52694400-52702800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr5:52694600-52696000 Weak transcription Muscle Satellite Cultured Cells --
12 chr5:52694600-52696000 Weak transcription NH-A brain
13 chr5:52695200-52696000 Weak transcription Hela-S3 cervix
14 chr5:52695200-52696400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr5:52695200-52696800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr5:52695800-52696400 Enhancers HSMM muscle
17 chr5:52695800-52696600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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