Variant report

Variant rs73365379
Chromosome Location chr14:105546642-105546643
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105542200-105548400 Weak transcription H9 Cell Line embryonic stem cell
2 chr14:105542400-105553400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr14:105544200-105547800 Weak transcription Primary B cells from peripheral blood blood
4 chr14:105544400-105547600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr14:105544400-105553000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:105544600-105548000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
7 chr14:105546200-105546800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr14:105546400-105546800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr14:105546400-105546800 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
10 chr14:105546400-105546800 Flanking Bivalent TSS/Enh NHEK skin
11 chr14:105546400-105547200 Enhancers A549 lung
12 chr14:105546600-105546800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr14:105546600-105546800 Bivalent Enhancer NHDF-Ad bronchial

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