chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107946242107947GGT6GENIChomozygous712881348
1242107964242107965GGA8GENIChomozygous712881349
1242108561242108562TC27GENIChomozygous573140468
1242109616242109617AG26GENIChomozygous573140469
1242109688242109689T-4GENIChomozygous712881350
1242111737242111738GGCA14GENICheterozygous712881353
1242111737242111738GGCACACACA14GENICpossibly homozygous712881355
1242111893242111894GGA22GENICpossibly homozygous712881356
1242112448242112449AAC6GENIChomozygous712881357
1242112822242112823GA26GENIChomozygous575233909
1242113547242113548CT46GENIChomozygous573140470
1242114398242114399AATC13GENIChomozygous712881358
1242114516242114517GGT14GENICheterozygous712881359
1242114516242114517GGTT14GENICheterozygous712881360
1242115682242115683CA28GENIChomozygous573140471