Variant report

Variant rs9688408
Chromosome Location chr6:132763644-132763645
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132736800-132764600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr6:132757800-132764600 Weak transcription NHDF-Ad bronchial
3 chr6:132760000-132767200 Weak transcription Primary B cells from cord blood blood
4 chr6:132761200-132763800 Weak transcription Osteobl bone
5 chr6:132761200-132764800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr6:132761200-132764800 Weak transcription HSMM muscle
7 chr6:132761400-132764800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr6:132761400-132766400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:132761600-132764800 Weak transcription NHLF lung
10 chr6:132762600-132778000 Weak transcription Aorta Aorta
11 chr6:132762600-132778000 Weak transcription Gastric stomach
12 chr6:132763000-132764000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr6:132763000-132764200 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr6:132763600-132764600 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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