Variant report

Variant rs545779125
Chromosome Location chr9:141042286-141042287
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140988200-141044600 Weak transcription Right Atrium heart
2 chr9:141041800-141042400 Enhancers K562 blood
3 chr9:141042200-141042400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr9:141042200-141042400 Enhancers Primary B cells from peripheral blood blood
5 chr9:141042200-141042400 Bivalent/Poised TSS Fetal Muscle Leg muscle
6 chr9:141042200-141042400 Active TSS Placenta Placenta
7 chr9:141042200-141042600 Active TSS HUES6 Cell Line embryonic stem cell
8 chr9:141042200-141042600 Active TSS iPS-15b Cell Line embryonic stem cell
9 chr9:141042200-141042600 Enhancers Primary neutrophils fromperipheralblood blood
10 chr9:141042200-141042600 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:141042200-141042600 Bivalent/Poised TSS Fetal Stomach stomach
12 chr9:141042200-141042600 Enhancers Ovary ovary
13 chr9:141042200-141042600 Active TSS HepG2 liver

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