Variant report

Variant rs7846749
Chromosome Location chr9:21780251-21780252
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21778400-21782200 Weak transcription Stomach Mucosa stomach
2 chr9:21778400-21782400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr9:21779000-21781000 Weak transcription NHEK skin
4 chr9:21779000-21781400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr9:21779600-21781400 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr9:21779600-21781400 Weak transcription Hela-S3 cervix
7 chr9:21779600-21788800 Weak transcription NHDF-Ad bronchial
8 chr9:21779800-21781400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr9:21779800-21782200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr9:21779800-21788600 Weak transcription NH-A brain
11 chr9:21780000-21781200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr9:21780000-21781400 Weak transcription HMEC breast
13 chr9:21780200-21781600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:21780200-21788600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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