chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15311391311393TG18GENICheterozygous141097136
15528838528839G6GENICheterozygous403368959
15528838528839GC6GENICheterozygous403368960
15552596552597A11GENICheterozygous403368969
15552596552597AG11GENICheterozygous403368970
15631900631900T18GENICheterozygous141097137
15659392659393T12GENICheterozygous141097138
15694955694959ATAC14GENICheterozygous141097139
15719829719830G17GENICheterozygous403368983
15719829719830GA17GENICpossibly homozygous403368984
15752007752008AG12GENICheterozygous154931878
15752007752008A12GENICheterozygous403656536
15752076752077G17GENICheterozygous403853457
15752076752077GC17GENICheterozygous403853458
15955325955326G20GENICheterozygous403743172
15955325955326GC20GENICheterozygous403743173
15589543589544GT10GENIChomozygous139652049