Variant report

Variant rs437389
Chromosome Location chr9:6099531-6099532
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:6096400-6100000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr9:6096400-6100200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:6096400-6100200 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr9:6096400-6100400 Enhancers HMEC breast
5 chr9:6096600-6100200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr9:6098400-6101800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:6098400-6102400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr9:6098800-6101000 Weak transcription Hela-S3 cervix
9 chr9:6098800-6101800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr9:6098800-6105200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:6099000-6100200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr9:6099200-6101800 Weak transcription NHDF-Ad bronchial
13 chr9:6099200-6102200 Weak transcription HUVEC blood vessel
14 chr9:6099200-6106600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr9:6099400-6101600 Weak transcription NHEK skin

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