chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT22GENIChomozygous701250227
99073349690733497GGT25GENIChomozygous701250228
99073384490733846GT--5GENICheterozygous701250230
99073588290735884GT--18GENICheterozygous701250232
99073603090736031TTGGGA30GENIChomozygous701250236
99073603290736033TG30GENIChomozygous551102279
99073687890736879TG26GENIChomozygous549954372
99073692190736922TG27GENIChomozygous549954373
99073693290736933TG27GENIChomozygous549954374
99073694690736947AG26GENIChomozygous549954375
99073695490736955TG26GENIChomozygous549954376
99073697190736972TA25GENIChomozygous549954377
99073856290738563TC16GENIChomozygous551102280
99074061090740612AT--1GENIChomozygous701250237
99074145590741456AAAGG17GENIChomozygous701250238
99074242690742428AA--5GENIChomozygous701250239
99074258390742584CT10GENIChomozygous551102281
99074258590742586TC11GENIChomozygous551102282
99074259990742600CA22GENIChomozygous551102283
99074260190742602GT22GENIChomozygous551102284
99074260490742606CC--22GENIChomozygous701250240
99074261090742611CT23GENIChomozygous551102285
99074261190742612CA23GENIChomozygous551102286
99074280890742809AAG6GENIChomozygous701250241
99074769090747691TTAG18GENIChomozygous701250242
99074795090747951CT31GENIChomozygous551102287
99074869490748696GT--7GENICheterozygous701250244