Variant report

Variant rs10177182
Chromosome Location chr2:186973078-186973079
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:186962600-186973400 Weak transcription Pancreas Pancrea
2 chr2:186966200-186980800 Weak transcription Small Intestine intestine
3 chr2:186970400-186981400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:186972200-186974000 Enhancers HepG2 liver
5 chr2:186972400-186973800 Enhancers Liver Liver

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