chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141246476141246477TC21GENIChomozygous69180442
7141246502141246503CA21GENIChomozygous69180443
7141247268141247269CT11GENIChomozygous69180444
7141247856141247857GA18GENIChomozygous69180445
7141247891141247892TG24GENIChomozygous69180446
7141248371141248372TA7GENIChomozygous69180447
7141248480141248481CA11GENIChomozygous69180448
7141248601141248602TC5GENIChomozygous69180449
7141248664141248665TC11GENIChomozygous69180453
7141248689141248690CG23GENIChomozygous69180454
7141249540141249541CT16GENIChomozygous69180455
7141250499141250500TC12GENIChomozygous69180456
7141250806141250807AG33GENIChomozygous69180457
7141250944141250945AG13GENIChomozygous69180458