Variant report

Variant rs76741474
Chromosome Location chr6:145389287-145389288
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145386200-145391800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:145388000-145393000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr6:145388000-145393200 Enhancers NHDF-Ad bronchial
4 chr6:145388200-145389400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr6:145388200-145389400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:145388200-145389400 Enhancers HMEC breast
7 chr6:145388200-145389400 Enhancers Osteobl bone
8 chr6:145388200-145389600 Enhancers Muscle Satellite Cultured Cells --
9 chr6:145388200-145393200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr6:145388600-145389400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:145388800-145389400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr6:145388800-145389400 Enhancers Hela-S3 cervix
13 chr6:145389000-145389400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr6:145389000-145389400 Enhancers NHLF lung

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