chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243703066243703067CT21GENICpossibly homozygous60087636
2243703891243703892AG4GENICheterozygous59472311
2243703899243703900GA4GENICheterozygous60087637
2243704226243704227GT1GENIChomozygous60462656
2243704677243704678GA11GENIChomozygous59472315
2243706074243706075AG23GENIChomozygous59472322
2243706468243706469AG26GENICpossibly homozygous59472323
2243707930243707931TC20GENICpossibly homozygous59472326
2243708087243708088GC12GENIChomozygous59472327
2243713323243713324C-21GENIChomozygous59472333
2243713389243713390C-9GENIChomozygous59472334