chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117455471117455472GA41GENIChomozygous970214885
8117457276117457277TA28GENICpossibly homozygous970214886
8117457763117457764CT26GENIChomozygous970214887
8117457819117457820TG38GENIChomozygous970214888
8117457980117457981AG33GENIChomozygous970214889
8117458100117458101CT35GENIChomozygous970214890
8117458667117458668CT32GENIChomozygous970214891
8117459094117459095TC32GENIChomozygous970214892
8117459216117459217GA23GENIChomozygous970214893
8117459485117459486AT23GENIChomozygous970214894
8117459675117459676AG44GENIChomozygous970214895
8117460438117460439TG23GENIChomozygous970214896
8117460566117460567GA37GENIChomozygous970214897
8117460641117460642GA27GENIChomozygous970214898
8117460884117460885CT40GENIChomozygous970214899
8117461267117461268TA22GENIChomozygous970214900
8117461352117461353GA36GENIChomozygous970214901
8117461374117461375TC29GENIChomozygous970214902
8117462087117462088AG28GENIChomozygous970214903
8117463688117463689AG26GENIChomozygous970214904
8117464601117464602TC28GENIChomozygous970214905
8117466249117466250AC30GENIChomozygous970214906
8117467952117467953AG21GENIChomozygous970214907
8117469362117469363TC32GENIChomozygous970214908
8117469784117469785CT22GENIChomozygous970214909
8117475110117475111CA27GENIChomozygous970214910