Variant report

Variant rs150843460
Chromosome Location chr5:178936514-178936515
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178933000-178943200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr5:178934600-178936800 Enhancers Primary B cells from cord blood blood
3 chr5:178934600-178937000 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr5:178934800-178937000 Enhancers Primary hematopoietic stem cells blood
5 chr5:178935000-178937000 Enhancers Primary neutrophils fromperipheralblood blood
6 chr5:178935400-178937200 Enhancers Primary monocytes fromperipheralblood blood
7 chr5:178936000-178936800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr5:178936000-178936800 Enhancers Fetal Kidney kidney
9 chr5:178936400-178936600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr5:178936400-178936600 Enhancers Fetal Stomach stomach
11 chr5:178936400-178936600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr5:178936400-178936800 Enhancers Primary B cells from peripheral blood blood
13 chr5:178936400-178936800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr5:178936400-178936800 Enhancers Thymus Thymus
15 chr5:178936400-178937000 Enhancers Fetal Lung lung

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