Variant report

Variant rs2282258
Chromosome Location chr9:139649612-139649613
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139648000-139650200 Enhancers Primary B cells from cord blood blood
2 chr9:139648000-139658200 Enhancers Primary B cells from peripheral blood blood
3 chr9:139648200-139649800 Enhancers Primary Natural Killer cells fromperipheralblood blood
4 chr9:139648400-139650200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr9:139648400-139650200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:139648600-139650000 Enhancers Primary hematopoietic stem cells blood
7 chr9:139649200-139649800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr9:139649200-139650000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr9:139649200-139650000 Bivalent Enhancer HepG2 liver
10 chr9:139649400-139650000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr9:139649600-139650200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:139649600-139651400 Weak transcription Fetal Muscle Trunk muscle
13 chr9:139649600-139654800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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