Variant report

Variant rs567584598
Chromosome Location chr9:71722503-71722504
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:71701800-71735200 Weak transcription Primary T cells from cord blood blood
2 chr9:71712600-71735200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr9:71715000-71735000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:71719400-71724400 Weak transcription Gastric stomach
5 chr9:71720400-71735600 Weak transcription Left Ventricle heart
6 chr9:71720600-71735000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr9:71721200-71726400 Weak transcription Stomach Mucosa stomach
8 chr9:71721400-71734600 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr9:71722000-71722800 Enhancers HepG2 liver
10 chr9:71722000-71723000 Enhancers Osteobl bone
11 chr9:71722000-71727800 Weak transcription Placenta Placenta
12 chr9:71722200-71722600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:71722200-71722600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:71722200-71722600 Enhancers Fetal Lung lung
15 chr9:71722400-71723000 Enhancers Liver Liver

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