chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104528289745282898TG11GENIChomozygous51873236
104528312845283129GT11GENIChomozygous51873239
104528325345283254TC8GENIChomozygous51873242
104528337845283379AG3GENIChomozygous51873245
104528358545283586CT6GENICheterozygous51873248
104528495045284951C-12GENICpossibly homozygous51873257
104528580145285802CT13GENICpossibly homozygous51873260
104528587745285881TAGC----6GENIChomozygous51873263
104528598645285987CT5GENIChomozygous51873266
104528633145286332GA6GENICheterozygous51873269
104528683645286837TC12GENIChomozygous51873271
104528693945286940TC11GENICpossibly homozygous51873274
104528849845288499CG7GENIChomozygous51873277
104528928445289285CT16GENICpossibly homozygous51873280
104529095345290954TC2GENICheterozygous51873283
104529014845290149GA10GENIChomozygous52193246
104528398445283985AG7GENIChomozygous51442165