Variant report

Variant rs4740675
Chromosome Location chr9:251531-251532
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:219000-261400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr9:237200-257400 Weak transcription Primary B cells from cord blood blood
3 chr9:249000-251600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr9:249200-251800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:249400-257000 Weak transcription Primary T helper naive cells from peripheral blood blood
6 chr9:249400-257800 Weak transcription Primary B cells from peripheral blood blood
7 chr9:249400-257800 Weak transcription Primary hematopoietic stem cells blood
8 chr9:249400-257800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr9:250400-252000 Flanking Active TSS K562 blood
10 chr9:250400-256200 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr9:250600-253600 Strong transcription Monocytes-CD14+_RO01746 blood
12 chr9:251000-251600 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr9:251000-253800 Weak transcription Primary monocytes fromperipheralblood blood
14 chr9:251000-257800 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr9:251200-251800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr9:251200-253200 Weak transcription Fetal Adrenal Gland Adrenal Gland
17 chr9:251200-254800 Weak transcription Spleen Spleen
18 chr9:251400-251800 Flanking Active TSS Breast Myoepithelial Primary Cells Breast

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