Variant report

Variant rs59212517
Chromosome Location chr9:84749355-84749356
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:84747000-84750400 Weak transcription Primary B cells from cord blood blood
2 chr9:84748200-84749600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr9:84748400-84750000 Enhancers HUVEC blood vessel
4 chr9:84748800-84749400 Enhancers Osteobl bone
5 chr9:84749000-84749400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr9:84749000-84749400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:84749000-84749600 Enhancers NHDF-Ad bronchial
8 chr9:84749200-84749400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr9:84749200-84749400 Enhancers Cortex derived primary cultured neurospheres brain
10 chr9:84749200-84749600 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr9:84749200-84749600 Enhancers NH-A brain

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