Variant report

Variant rs66895129
Chromosome Location chr13:110572366-110572367
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110566800-110590400 Weak transcription Aorta Aorta
2 chr13:110569400-110573400 Enhancers HSMM muscle
3 chr13:110569600-110572400 Enhancers HSMMtube muscle
4 chr13:110569600-110573000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr13:110570800-110572400 Enhancers Adipose Nuclei Adipose
6 chr13:110570800-110572400 Enhancers Skeletal Muscle Male skeletal muscle
7 chr13:110570800-110574800 Weak transcription NHDF-Ad bronchial
8 chr13:110571000-110586000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr13:110571200-110574600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr13:110571400-110573000 Enhancers Muscle Satellite Cultured Cells --
11 chr13:110571800-110572600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr13:110572000-110572600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr13:110572000-110572600 Enhancers NHLF lung
14 chr13:110572000-110573000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr13:110572200-110572400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr13:110572200-110572600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr13:110572200-110573000 Enhancers NH-A brain

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