chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
615143041514305CT7GENIChomozygous115035526
615143361514337GA5GENIChomozygous115035528
615149751514976TG8GENIChomozygous115035530
615151261515127GA20GENIChomozygous115035532
615152511515252AG16GENIChomozygous115035534
615167241516725AT16GENIChomozygous115035536
615168451516846TG13GENICheterozygous118568193
615170131517014TC24GENIChomozygous115035544
615171151517116AC17GENIChomozygous115035546
615171541517155TC22GENIChomozygous115035548
615174821517483GA22GENIChomozygous115035550
615174841517485AG23GENIChomozygous115035552
615179161517917CT22GENIChomozygous115035554
615185691518570TA23GENIChomozygous115230397
615188301518831AG27GENIChomozygous115035556