Variant report

Variant rs7794881
Chromosome Location chr7:38296215-38296216
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:38273800-38305400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr7:38288200-38297000 Weak transcription Primary T killer memory cells from peripheral blood blood
3 chr7:38288200-38311200 Weak transcription Primary T cells from cord blood blood
4 chr7:38293600-38298000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr7:38295400-38302600 Genic enhancers Primary Natural Killer cells fromperipheralblood blood
6 chr7:38295600-38296600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr7:38295600-38297200 Enhancers Primary hematopoietic stem cells blood
8 chr7:38295600-38297600 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr7:38295600-38298600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr7:38295800-38296400 Enhancers Primary monocytes fromperipheralblood blood
11 chr7:38296000-38305200 Weak transcription Primary T cells fromperipheralblood blood
12 chr7:38296200-38297200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr7:38296200-38297400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
14 chr7:38296200-38297400 Enhancers Placenta Placenta
15 chr7:38296200-38297400 Enhancers Fetal Thymus thymus
16 chr7:38296200-38297400 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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