chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141714512317145124AG16GENIChomozygous48547698
141714523417145235CT3GENICheterozygous48547699
141714523717145238CT3GENICheterozygous48547700
141714543617145437AT8GENIChomozygous48547701
141714600917146010CG3GENICheterozygous49501608
141714601317146014CG6GENICheterozygous49501610
141714601717146018CG3GENICheterozygous49501612
141714602117146022CG6GENICheterozygous49501615
141714664517146649AATC----1GENIChomozygous48956516
141714688117146882TC9GENIChomozygous48547703
141714729217147293TA21GENIChomozygous48547704
141714759417147595TC21GENICpossibly homozygous48547705
141714859317148594A-3GENICheterozygous48956520
141714903817149039CT14GENICheterozygous48956524
141714929817149299TC8GENIChomozygous48547713
141714975317149754AG9GENIChomozygous48956526
141714976117149762AG10GENIChomozygous48956528
141714976317149764TG10GENIChomozygous48956530
141714981117149812AT20GENICpossibly homozygous48956532
141714986117149862AG23GENICpossibly homozygous48956534
141714990517149906CA17GENICpossibly homozygous48956536
141714997117149972AG13GENIChomozygous48956538
141715008017150081GA20GENICpossibly homozygous48956540
141715019217150193AG17GENICpossibly homozygous48956542