Variant report

Variant rs34591542
Chromosome Location chr4:166054556-166054557
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:166052000-166056600 Enhancers Primary B cells from peripheral blood blood
2 chr4:166053000-166054800 Weak transcription Fetal Brain Male brain
3 chr4:166053000-166055000 Enhancers Liver Liver
4 chr4:166053400-166057200 Weak transcription HepG2 liver
5 chr4:166053600-166054800 Flanking Active TSS Primary B cells from cord blood blood
6 chr4:166053600-166056000 Enhancers Primary hematopoietic stem cells blood
7 chr4:166053600-166056000 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr4:166053800-166056400 Enhancers Primary monocytes fromperipheralblood blood
9 chr4:166054000-166054600 Enhancers Fetal Brain Female brain
10 chr4:166054000-166054800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr4:166054000-166054800 Flanking Active TSS GM12878-XiMat blood
12 chr4:166054000-166055400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
13 chr4:166054000-166056200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr4:166054400-166054600 Enhancers Primary neutrophils fromperipheralblood blood

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