chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121801725318017254CT16GENICpossibly homozygous50719515
121802028418020285AG20GENIChomozygous50089211
121802102118021022CT23GENICpossibly homozygous50089213
121802301918023020AAAAAC2GENICheterozygous50719517
121802337318023374GGA3GENICheterozygous50282921
121802352018023521AC14GENICpossibly homozygous50089223
121802356118023562AAG3GENIChomozygous50719519
121802356218023563CT3GENIChomozygous50719521
121802356518023566GGTAGTC2GENIChomozygous50719523
121802468318024684GGA9GENICheterozygous50089227
121802493318024934A-1GENIChomozygous50089229
121802597818025979AG8GENICpossibly homozygous50506953
121802682618026828TA--13GENIChomozygous50089231
121802882518028826GT27GENIChomozygous50719525
121802919718029198AT15GENICheterozygous50719527
121802940018029401CT9GENICheterozygous50719529
121802945218029453AC5GENICheterozygous50089241
121803133218031333GA3GENICheterozygous50089245
121803218418032185GA11GENIChomozygous50719531
121803437518034376TA3GENICheterozygous50089253