chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217018931217018932AC7GENIChomozygous108536537
1217020176217020177AG24GENIChomozygous108992491
1217020245217020246AC23GENIChomozygous108536539
1217020420217020421GA17GENIChomozygous108992492
1217020825217020826AG14GENIChomozygous108992493
1217020852217020853GA15GENIChomozygous108536540
1217021048217021049AG20GENIChomozygous108536541
1217021857217021858TG25GENIChomozygous108992494
1217022040217022041AG20GENIChomozygous108992495
1217022220217022221AG25GENIChomozygous108992496
1217023556217023557AG7GENIChomozygous108536544
1217024452217024453TC14GENIChomozygous108536548
1217027134217027135GA32GENIChomozygous108992497
1217027844217027845GA19GENIChomozygous108536554
1217028768217028769AG27GENIChomozygous108536556
1217029411217029412TC14GENIChomozygous108536557
1217029771217029772GA24GENIChomozygous108536558
1217030490217030491AC23GENIChomozygous108992498
1217032206217032207CA24GENIChomozygous108992499
1217032371217032372CG15GENIChomozygous108992500
1217032606217032607AG28GENIChomozygous108536567