Variant report

Variant rs73668368
Chromosome Location chr9:139650186-139650187
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 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 chr9:139648400-139650200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr9:139648400-139650200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr9:139649600-139650200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
6 chr9:139649600-139651400 Weak transcription Fetal Muscle Trunk muscle
7 chr9:139649600-139654800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr9:139650000-139651000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:139650000-139651000 ZNF genes & repeats Skeletal Muscle Male skeletal muscle
10 chr9:139650000-139655200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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