Variant report

Variant rs569587200
Chromosome Location chr14:78786599-78786600
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:78779200-78787000 Enhancers Brain Germinal Matrix brain
2 chr14:78783200-78794000 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr14:78785200-78787000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr14:78785400-78787200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr14:78785600-78786600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr14:78786000-78786600 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr14:78786000-78786800 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr14:78786200-78786800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr14:78786200-78786800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr14:78786400-78786600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr14:78786400-78786800 Flanking Active TSS K562 blood

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