Variant report

Variant rs11175546
Chromosome Location chr12:40587815-40587816
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:40586000-40591000 Enhancers Primary neutrophils fromperipheralblood blood
2 chr12:40586200-40591600 Enhancers Primary monocytes fromperipheralblood blood
3 chr12:40586800-40588800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr12:40587000-40588000 Weak transcription Primary hematopoietic stem cells blood
5 chr12:40587000-40588200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr12:40587200-40588000 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr12:40587200-40588200 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr12:40587200-40588200 Enhancers Primary B cells from cord blood blood
9 chr12:40587200-40589400 Weak transcription HUVEC blood vessel
10 chr12:40587200-40590400 Enhancers Primary B cells from peripheral blood blood
11 chr12:40587400-40588000 Enhancers GM12878-XiMat blood
12 chr12:40587600-40588000 Weak transcription Primary hematopoietic stem cells short term culture blood
13 chr12:40587600-40588200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr12:40587600-40588200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr12:40587800-40588000 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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