chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT4GENIChomozygous769059684
99073349690733497GGT13GENIChomozygous769059685
99073474190734742GA27GENICpossibly homozygous671514375
99073573190735732AAGT5GENICheterozygous769059686
99073639590736396TG16GENICpossibly homozygous671514376
99073687890736879TG16GENICpossibly homozygous671514377
99073692190736922TG11GENIChomozygous671514378
99073693290736933TG4GENIChomozygous671514379
99073694690736947AG2GENIChomozygous671514380
99073695490736955TG3GENIChomozygous671514381
99073697190736972TA7GENIChomozygous671514382
99073982890739830AA--7GENIChomozygous769059687
99074134590741346GA12GENICheterozygous671514383
99074242490742426TT--2GENIChomozygous769059688
99074261090742611CT2GENIChomozygous671514384
99074261190742612CA2GENIChomozygous671514385
99074383790743838CT28GENIChomozygous671514386
99074429890744299TTC4GENIChomozygous769059689
99074517990745180AT6GENICheterozygous671514387
99074558690745587TG19GENIChomozygous671514388
99074564590745646AT11GENICpossibly homozygous671514389
99074575390745754TA13GENICheterozygous671514390
99074595590745956AAC10GENIChomozygous769059690
99074595690745957AT11GENIChomozygous671514391
99074649690746497AC18GENIChomozygous671514392
99074653390746534G-17GENIChomozygous769059691
99074821890748219GC3GENIChomozygous671514393
99074879190748792GGT24GENIChomozygous769059692
99074969590749696GA6GENICheterozygous671514394