chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897762678977627TC20GENIChomozygous965713485
17897870878978709CT24GENIChomozygous965713486
17897927378979274CT21GENIChomozygous965713487
17897938978979390CT19GENIChomozygous965713488
17898330978983310AT27GENIChomozygous965713489
17898368578983686GA23GENIChomozygous965713490
17898381078983811TC34GENIChomozygous965713491
17898490378984904CT29GENICpossibly homozygous965713492
17898747278987473GA26GENIChomozygous965713493
17898771378987714TC12GENIChomozygous965713494
17898904178989042TG32GENIChomozygous965713495
17899010278990103AG19GENIChomozygous965713496
17899258778992588AG13GENIChomozygous965713497
17899300878993009TC20GENIChomozygous965713498
17899399578993996CA4GENIChomozygous965713499
17899567078995671AT26GENIChomozygous965713500
17899644878996449TG16GENIChomozygous965713501
17899645278996453TC16GENIChomozygous965713502
17899711378997114AG20GENIChomozygous965713503