chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116730989116730990CCT13INTERGENIChomozygous52828603
8116732565116732566AG18GENIChomozygous52828604
8116734597116734603TTTTTT------2GENIChomozygous52828605
8116734979116734980GGT2GENICheterozygous52828606
8116734979116734980GGTT2GENICheterozygous52828607
8116739403116739404CCT5GENICheterozygous52828608
8116740144116740145A-3GENIChomozygous52828609
8116740295116740296CA26GENIChomozygous52828610
8116743143116743144A-11GENICpossibly homozygous52828611
8116743147116743148AC18GENICheterozygous52828612
8116746426116746427A-18GENICpossibly homozygous52828613
8116748668116748669CCA3GENICheterozygous52828614