Variant report

Variant rs11253060
Chromosome Location chr10:5276817-5276818
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5275000-5277800 Enhancers HepG2 liver
2 chr10:5275400-5277800 Enhancers Primary monocytes fromperipheralblood blood
3 chr10:5275600-5277000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr10:5275600-5277600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr10:5275600-5278000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr10:5275800-5277000 Enhancers Primary hematopoietic stem cells blood
7 chr10:5276000-5277000 Flanking Active TSS Primary neutrophils fromperipheralblood blood
8 chr10:5276000-5277000 Enhancers Stomach Mucosa stomach
9 chr10:5276200-5277000 Enhancers Adipose Nuclei Adipose
10 chr10:5276200-5277000 Enhancers Fetal Lung lung
11 chr10:5276200-5277000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr10:5276400-5277000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr10:5276400-5277200 Enhancers Placenta Placenta
14 chr10:5276400-5283600 Weak transcription A549 lung
15 chr10:5276600-5277000 Enhancers Esophagus oesophagus
16 chr10:5276600-5277000 Enhancers Lung lung
17 chr10:5276600-5277400 Enhancers Primary Natural Killer cells fromperipheralblood blood
18 chr10:5276800-5277200 Enhancers Primary hematopoietic stem cells short term culture blood
19 chr10:5276800-5280800 Weak transcription Gastric stomach

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