Variant report

Variant rs1374786
Chromosome Location chr3:160700496-160700497
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:160695200-160701400 Enhancers Primary monocytes fromperipheralblood blood
2 chr3:160696200-160700600 Enhancers Dnd41 blood
3 chr3:160697000-160704000 Weak transcription Stomach Smooth Muscle stomach
4 chr3:160697200-160710600 Weak transcription Left Ventricle heart
5 chr3:160697800-160701400 Enhancers Primary hematopoietic stem cells blood
6 chr3:160698200-160700800 Enhancers Primary B cells from peripheral blood blood
7 chr3:160698200-160700800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr3:160698200-160701000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr3:160699200-160701200 Enhancers Primary neutrophils fromperipheralblood blood
10 chr3:160699200-160701600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr3:160699400-160700600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr3:160699800-160701200 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr3:160699800-160701200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
14 chr3:160700000-160702000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
15 chr3:160700200-160701000 Weak transcription Adipose Nuclei Adipose
16 chr3:160700200-160701400 Weak transcription Placenta Placenta
17 chr3:160700400-160701200 Enhancers Primary B cells from cord blood blood

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