Variant report

Variant rs17661280
Chromosome Location chr19:52239829-52239830
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52237800-52244600 Enhancers Primary monocytes fromperipheralblood blood
2 chr19:52238200-52247000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr19:52238600-52240000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
4 chr19:52238600-52240600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
5 chr19:52238600-52243400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr19:52238800-52240400 Enhancers K562 blood
7 chr19:52239000-52240000 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr19:52239000-52240200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr19:52239000-52240200 Enhancers HSMMtube muscle
10 chr19:52239000-52240400 Enhancers Primary hematopoietic stem cells short term culture blood
11 chr19:52239000-52240400 Enhancers Muscle Satellite Cultured Cells --
12 chr19:52239000-52240400 Enhancers HSMM muscle
13 chr19:52239000-52240600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr19:52239400-52243000 Weak transcription NHDF-Ad bronchial
15 chr19:52239600-52240200 Enhancers Primary B cells from cord blood blood
16 chr19:52239800-52240400 Enhancers Osteobl bone
17 chr19:52239800-52251000 Weak transcription Primary hematopoietic stem cells blood

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