chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46916964969169650CA9GENIChomozygous113347995
46916972669169727GA10GENIChomozygous113347997
46916976269169763AG11GENIChomozygous112693745
46916983869169839AC17GENIChomozygous112693747
46917016869170169AC17GENIChomozygous112693749
46917031469170315CT11GENIChomozygous112693751
46917086469170865AG14GENIChomozygous112693753
46917091769170918GT11GENIChomozygous112693755
46917107769171078CT15GENIChomozygous112693757
46917112069171121TA13GENIChomozygous112693761
46917124069171241TC9GENIChomozygous112693763
46917175569171756TC12GENIChomozygous112693765
46917186069171861TC13GENIChomozygous113347999
46917192169171922CT14GENIChomozygous112693767
46917288369172884TC6GENIChomozygous112693773
46917314769173148AT7GENIChomozygous112693775
46917327869173279CT13GENIChomozygous112693777
46917335069173351TG12GENIChomozygous112693779
46917408769174088CT14GENIChomozygous112693785
46917411669174117GA18GENIChomozygous113348003
46917446469174465GA13GENIChomozygous112693791
46917448969174490AG11GENIChomozygous112693793
46917488369174884GA9GENIChomozygous113348005
46917490769174908TC11GENIChomozygous119277672
46917491069174911CT11GENIChomozygous119277674
46917507769175078CG13GENIChomozygous112693795
46917517369175174CA7GENIChomozygous112693797
46917529669175297TC10GENIChomozygous112693799
46917578469175785GA8GENIChomozygous112693801
46917595069175951CA11GENIChomozygous112693803
46917632369176324TC9GENIChomozygous112693805
46917652969176530AG9GENIChomozygous112693807
46917655469176555GT9GENIChomozygous113348007
46917655669176557GT9GENIChomozygous112693809
46917664069176641GC8GENIChomozygous112693811
46917711169177112TG4GENIChomozygous112693813
46917718269177183AC9GENIChomozygous112693817
46917725469177255AG8GENIChomozygous112693819
46917735969177360AG9GENIChomozygous112693821
46917758069177581AG11GENIChomozygous112693823
46917763769177638GC9GENIChomozygous112693825
46917795569177956TA13GENIChomozygous112693827
46917810969178110AT8GENIChomozygous112693829