chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116724205867242059AG45GENIChomozygous50883226
116724245067242451TG75GENIChomozygous50807788
116724367167243672GC55GENICpossibly homozygous50883228
116724478267244783GGT64GENIChomozygous50807789
116724499667244999AAT---45GENIChomozygous50807790
116724520667245212TCTCTC------14GENICheterozygous50883230
116724537067245371CT18GENIChomozygous50883232
116724537167245372CCTCACACTT18GENIChomozygous50807793
116724539467245395CT23GENIChomozygous50807795
116724544067245441CA44GENIChomozygous50807797
116724570867245714AAAAAG------46GENIChomozygous50807800
116724588967245890AT43GENIChomozygous50807802
116724655767246558TC63GENIChomozygous50807803
116724688567246886TTG38GENIChomozygous50807810
116724701467247015AG54GENIChomozygous50807813
116724702067247021CT54GENIChomozygous50807815
116724703367247034TC61GENIChomozygous50807816
116724712367247124TC69GENIChomozygous50807818
116724722267247223A-40GENIChomozygous50807819
116724723267247233CG43GENIChomozygous50807821
116724734967247350TG60GENIChomozygous50807822
116724768967247691GT--50GENIChomozygous50807823