chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109118776991187770GA28GENIChomozygous138848546
109118820991188210AG25GENIChomozygous143466428
109118899291188993GT17GENIChomozygous138848547
109118907191189072TC19GENIChomozygous138848548
109118909891189099CT23GENICpossibly homozygous138848549
109118910991189110CA23GENICpossibly homozygous138848550
109119032791190328TC16GENIChomozygous143466429
109119088191190882GA18GENIChomozygous143466430
109119147391191474CG16GENIChomozygous138848552
109119187691191877GC16GENIChomozygous138848553
109119234191192342GA22GENIChomozygous143466431
109119253491192535AG20GENIChomozygous138848554
109119266891192669AG13GENIChomozygous138848555