Variant report

Variant rs7022856
Chromosome Location chr9:21788523-21788524
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21779600-21788800 Weak transcription NHDF-Ad bronchial
2 chr9:21779800-21788600 Weak transcription NH-A brain
3 chr9:21780200-21788600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr9:21786800-21789200 Weak transcription Primary neutrophils fromperipheralblood blood
5 chr9:21787600-21789200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr9:21787800-21789000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:21787800-21789800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr9:21788000-21788600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:21788200-21788600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:21788200-21789800 Enhancers HMEC breast
11 chr9:21788200-21790200 Enhancers Hela-S3 cervix
12 chr9:21788200-21790200 Enhancers NHEK skin
13 chr9:21788400-21788600 Enhancers A549 lung
14 chr9:21788400-21788800 Enhancers Osteobl bone

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