Variant report

Variant rs10993911
Chromosome Location chr9:136935697-136935698
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:136934400-136936000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr9:136934800-136936000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr9:136934800-136936200 Bivalent Enhancer HepG2 liver
4 chr9:136935400-136936000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr9:136935600-136935800 Enhancers Primary hematopoietic stem cells blood
6 chr9:136935600-136935800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr9:136935600-136935800 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle

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