Variant report

Variant rs7439792
Chromosome Location chr4:69959599-69959600
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69957400-69959600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr4:69957400-69960000 Enhancers NHEK skin
3 chr4:69957600-69959800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr4:69958000-69960800 Weak transcription HUVEC blood vessel
5 chr4:69958200-69961000 Weak transcription HMEC breast
6 chr4:69958400-69961800 Weak transcription Osteobl bone
7 chr4:69958800-69959600 Enhancers Muscle Satellite Cultured Cells --
8 chr4:69958800-69959600 Enhancers NH-A brain
9 chr4:69959000-69959600 ZNF genes & repeats Fetal Intestine Small intestine
10 chr4:69959200-69959600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr4:69959200-69961000 Enhancers A549 lung
12 chr4:69959400-69959600 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr4:69959400-69959600 Enhancers HepG2 liver
14 chr4:69959400-69960400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr4:69959400-69960800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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