Variant report

Variant rs73553043
Chromosome Location chr6:133944784-133944785
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:133942200-133945800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
2 chr6:133942200-133945800 Enhancers Muscle Satellite Cultured Cells --
3 chr6:133942400-133945200 Enhancers Adipose Nuclei Adipose
4 chr6:133942400-133945200 Enhancers HSMM muscle
5 chr6:133942400-133945400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr6:133942400-133945800 Enhancers Fetal Stomach stomach
7 chr6:133942600-133945200 Enhancers NHDF-Ad bronchial
8 chr6:133942600-133945800 Enhancers Osteobl bone
9 chr6:133942800-133945200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr6:133942800-133945200 Enhancers A549 lung
11 chr6:133942800-133948400 Enhancers Fetal Lung lung
12 chr6:133943600-133944800 Enhancers Aorta Aorta
13 chr6:133943600-133945400 Enhancers Ovary ovary
14 chr6:133944000-133945200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr6:133944400-133944800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr6:133944400-133945400 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr6:133944400-133951800 Weak transcription NH-A brain
18 chr6:133944400-133962000 Weak transcription Fetal Kidney kidney
19 chr6:133944600-133945000 Active TSS Right Atrium heart
20 chr6:133944600-133952400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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