Variant report

Variant rs138874604
Chromosome Location chr5:119730920-119730921
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:119724600-119735200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr5:119725000-119731800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr5:119725600-119732000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr5:119725800-119731400 Weak transcription NHDF-Ad bronchial
5 chr5:119727400-119733600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr5:119730800-119731400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr5:119730800-119733200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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