Variant report

Variant rs59462456
Chromosome Location chr10:19991209-19991210
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:19986800-20000400 Weak transcription Fetal Intestine Small intestine
2 chr10:19988400-19993200 Weak transcription Fetal Intestine Large intestine
3 chr10:19989200-20000400 Weak transcription Duodenum Mucosa Duodenum
4 chr10:19990400-19991800 Enhancers HSMMtube muscle
5 chr10:19990800-19991400 Enhancers NH-A brain
6 chr10:19990800-19991800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr10:19990800-19991800 Enhancers Muscle Satellite Cultured Cells --
8 chr10:19990800-19991800 Enhancers NHEK skin
9 chr10:19990800-19991800 Enhancers Osteobl bone
10 chr10:19990800-19992000 Enhancers HSMM muscle
11 chr10:19991000-19991400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr10:19991200-19991400 Enhancers Aorta Aorta

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