Variant report

Variant rs10456122
Chromosome Location chr6:45163057-45163058
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:45159600-45163800 Weak transcription Liver Liver
2 chr6:45160000-45167000 Weak transcription Fetal Intestine Small intestine
3 chr6:45160200-45166000 Weak transcription HepG2 liver
4 chr6:45160600-45167000 Weak transcription Fetal Intestine Large intestine
5 chr6:45162000-45171800 Enhancers Dnd41 blood
6 chr6:45162800-45163200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr6:45162800-45163400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr6:45163000-45163200 Enhancers Primary T killer naive cells fromperipheralblood blood
9 chr6:45163000-45163200 Enhancers Pancreatic Islets Pancreatic Islet
10 chr6:45163000-45163200 Enhancers Psoas Muscle Psoas
11 chr6:45163000-45164800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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