Variant report

Variant rs10887951
Chromosome Location chr10:91144909-91144910
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:91135000-91150200 Weak transcription Fetal Brain Male brain
2 chr10:91141000-91150000 Weak transcription Fetal Heart heart
3 chr10:91143400-91146000 Enhancers Primary monocytes fromperipheralblood blood
4 chr10:91143400-91146400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr10:91143800-91145600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
6 chr10:91144000-91145600 Enhancers Primary B cells from peripheral blood blood
7 chr10:91144200-91145200 Flanking Active TSS Primary hematopoietic stem cells blood
8 chr10:91144400-91145000 Flanking Active TSS Primary neutrophils fromperipheralblood blood
9 chr10:91144400-91145400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr10:91144600-91145400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr10:91144600-91145400 Enhancers Primary mononuclear cells fromperipheralblood Blood
12 chr10:91144600-91145600 Flanking Active TSS Primary hematopoietic stem cells short term culture blood
13 chr10:91144800-91145400 Enhancers GM12878-XiMat blood
14 chr10:91144800-91145600 Enhancers Primary B cells from cord blood blood
15 chr10:91144800-91146600 Enhancers HUES6 Cell Line embryonic stem cell
16 chr10:91144800-91146600 Enhancers HUES64 Cell Line embryonic stem cell

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