chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116724245067242451TG24GENIChomozygous50807788
116724478267244783GGT27GENIChomozygous50807789
116724499667244999AAT---5GENIChomozygous50807790
116724537067245371CT18GENIChomozygous50883232
116724537167245372CCTCACACTT18GENIChomozygous50807793
116724539467245395CT24GENIChomozygous50807795
116724544067245441CA29GENIChomozygous50807797
116724568467245685AC16GENIChomozygous50807798
116724568567245686GA16GENIChomozygous51187217
116724569067245691GGA13GENIChomozygous51187218
116724570867245714AAAAAG------15GENIChomozygous50807800
116724588967245890AT13GENIChomozygous50807802
116724655767246558TC36GENIChomozygous50807803
116724701467247015AG43GENIChomozygous50807813
116724702067247021CT45GENIChomozygous50807815
116724703367247034TC44GENIChomozygous50807816
116724712367247124TC39GENIChomozygous50807818
116724722267247223A-21GENIChomozygous50807819
116724723267247233CG22GENIChomozygous50807821
116724734967247350TG16GENIChomozygous50807822
116724768967247691GT--28GENIChomozygous50807823