chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104528289745282898TG14GENIChomozygous51873236
104528312845283129GT18GENIChomozygous51873239
104528325345283254TC15GENICpossibly homozygous51873242
104528337845283379AG8GENICpossibly homozygous51873245
104528358545283586CT20GENICpossibly homozygous51873248
104528384045283841CG5GENIChomozygous51985876
104528398445283985AG16GENICpossibly homozygous51442165
104528435645284357TC6GENIChomozygous51873251
104528449745284498CT4GENICheterozygous51873254
104528495045284951C-22GENICpossibly homozygous51873257
104528580145285802CT29GENICpossibly homozygous51873260
104528587745285881TAGC----11GENIChomozygous51873263
104528598645285987CT14GENICpossibly homozygous51873266
104528633145286332GA11GENICheterozygous51873269
104528683645286837TC21GENIChomozygous51873271
104528693945286940TC12GENICpossibly homozygous51873274
104528849845288499CG16GENICpossibly homozygous51873277
104528928445289285CT26GENIChomozygous51873280
104529014845290149GA12GENIChomozygous52193246
104529095345290954TC20GENICpossibly homozygous51873283