chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1195076468195076469TC15GENIChomozygous108475133
1195081941195081942T17GENIChomozygous130829664
1195085845195085846AG13GENIChomozygous108978717
1195086688195086689CA23GENIChomozygous108978720
1195080102195080103GC24GENIChomozygous120584496
1195081077195081078AG14GENIChomozygous120584498
1195081400195081401TC12GENIChomozygous120584500
1195082985195082986GA22GENIChomozygous120584502
1195083102195083103TG11GENICpossibly homozygous120584504
1195083439195083440TC18GENIChomozygous120584506
1195087423195087424T20GENICpossibly homozygous129844283
1195087743195087744TG23GENIChomozygous108978724
1195091300195091301CA21GENIChomozygous108978725
1195087491195087491TTGA9GENIChomozygous127469661
1195087486195087490CCCA9GENIChomozygous127469660
1195088486195088488AA23GENIChomozygous130829667
1195091531195091532GA18GENIChomozygous120584508
1195091927195091928TC27GENIChomozygous108978727
1195092124195092125TG22GENIChomozygous108978728
1195093268195093269TA20GENIChomozygous120584510
1195094020195094021AG18GENIChomozygous108978730
1195094943195094944AG10GENIChomozygous108978731
1195096097195096098TC16GENIChomozygous108978735
1195096174195096175CG14GENIChomozygous120889298
1195095098195095099G20GENIChomozygous131263269
1195096160195096161C12GENIChomozygous131263270
1195096168195096169CA13GENIChomozygous120889297