Variant report

Variant rs4691159
Chromosome Location chr4:166053627-166053628
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:166051400-166054000 Weak transcription GM12878-XiMat blood
2 chr4:166051600-166053800 Weak transcription Primary monocytes fromperipheralblood blood
3 chr4:166052000-166056600 Enhancers Primary B cells from peripheral blood blood
4 chr4:166052400-166054000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr4:166053000-166053800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr4:166053000-166054000 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr4:166053000-166054800 Weak transcription Fetal Brain Male brain
8 chr4:166053000-166055000 Enhancers Liver Liver
9 chr4:166053200-166053800 Weak transcription Brain Hippocampus Middle brain
10 chr4:166053400-166057200 Weak transcription HepG2 liver
11 chr4:166053600-166054000 Enhancers Monocytes-CD14+_RO01746 blood
12 chr4:166053600-166054200 Enhancers Primary neutrophils fromperipheralblood blood
13 chr4:166053600-166054800 Flanking Active TSS Primary B cells from cord blood blood
14 chr4:166053600-166056000 Enhancers Primary hematopoietic stem cells blood
15 chr4:166053600-166056000 Enhancers Primary hematopoietic stem cells short term culture blood

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