chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121900036119000362GA22GENIChomozygous126241062
121900240719002408TC6GENIChomozygous126241064
121900270819002709AC8GENIChomozygous126241066
121900304119003042AG7GENIChomozygous126168364
121900537419005375CT13GENIChomozygous126241068
121900545119005452CT19GENIChomozygous126241070
121900601419006015GA13GENIChomozygous126241072
121900702019007021TC9GENIChomozygous126241074
121900764719007648AG9GENIChomozygous126168372
121900844719008448CA16GENIChomozygous126168375
121900936019009361TA12GENIChomozygous126241076
121900950219009503GC10GENIChomozygous126241078
121901242619012427TA4GENICheterozygous126241080
121901583819015839CT22GENIChomozygous126241082
121902166319021664AG6GENICheterozygous126210111
121902174419021745AC4GENICheterozygous126241084
121902174519021746AC4GENIChomozygous126241086
121902486519024866GA22GENICpossibly homozygous126168404
121902506619025067CG21GENIChomozygous126241088
121902511419025115CT18GENIChomozygous126241090
121902539819025399GA8GENIChomozygous126241092
121902747619027477TC14GENIChomozygous126210115
121902894319028944AC19GENIChomozygous126241094
121902903919029040CT21GENIChomozygous126168415
121902948819029489GA25GENIChomozygous126168416
121903221619032217GA11GENIChomozygous126241096
121903238719032388AG7GENIChomozygous126168417