Variant report

Variant rs543900890
Chromosome Location chr10:5076280-5076281
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5068000-5076800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr10:5074000-5078800 Weak transcription Stomach Mucosa stomach
3 chr10:5074800-5076600 Enhancers Hela-S3 cervix
4 chr10:5075000-5076400 Enhancers HMEC breast
5 chr10:5075000-5076800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr10:5075000-5076800 Enhancers Muscle Satellite Cultured Cells --
7 chr10:5075200-5076600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr10:5075200-5076600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr10:5075200-5076600 Enhancers NH-A brain
10 chr10:5075200-5077000 ZNF genes & repeats Adipose Nuclei Adipose
11 chr10:5075600-5076800 Enhancers Osteobl bone
12 chr10:5076000-5076800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr10:5076200-5077400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr10:5076200-5080800 Weak transcription NHDF-Ad bronchial

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