chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127980705127980706GA38GENIChomozygous52884546
8127980741127980742CCG20GENIChomozygous52884547
8127981050127981051AC44GENICpossibly homozygous52884548
8127981103127981104TC39GENIChomozygous52884549
8127981148127981149AG43GENIChomozygous52884550
8127981289127981301GAATGAATGAAT------------6GENIChomozygous52884551
8127981489127981490GGA11GENIChomozygous52884552
8127981674127981675CG35GENIChomozygous52884553
8127981931127981933AC--14GENICheterozygous52884555
8127981939127981941AC--15GENICheterozygous52884556
8127982286127982287GA37GENIChomozygous52884558
8127982327127982328TC31GENIChomozygous52884559
8127982384127982385TC37GENIChomozygous52884560
8127982540127982541CT25GENIChomozygous52884561
8127983068127983069GA38GENIChomozygous52884562
8127983218127983219CT35GENIChomozygous52884563