chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111676152111676153TC25GENIChomozygous116648544
8111676535111676536TC23GENIChomozygous116648546
8111676727111676728AC21GENIChomozygous116648548
8111677564111677565TC21GENIChomozygous116648550
8111677792111677793AG18GENIChomozygous116648552
8111678092111678093CT18GENIChomozygous116648554
8111678149111678150AG19GENIChomozygous116648556
8111678156111678157GC19GENIChomozygous116648558
8111679047111679048CG32GENIChomozygous116648560
8111680019111680020TC24GENIChomozygous116648562
8111680058111680059TC27GENICpossibly homozygous116648564
8111682019111682020AG38GENIChomozygous116648566
8111682438111682439AG14GENIChomozygous116648570
8111682504111682505GT22GENIChomozygous117172926
8111683450111683451TC29GENIChomozygous116648572
8111684688111684689AG14GENIChomozygous116648574
8111685486111685487CT25GENIChomozygous116648578
8111685985111685986AG20GENIChomozygous116648580