chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141246476141246477TC21GENIChomozygous69180442
7141246502141246503CA19GENICpossibly homozygous69180443
7141247268141247269CT36GENIChomozygous69180444
7141247856141247857GA44GENIChomozygous69180445
7141247891141247892TG45GENICpossibly homozygous69180446
7141248371141248372TA25GENIChomozygous69180447
7141248480141248481CA12GENIChomozygous69180448
7141248664141248665TC4GENIChomozygous69180453
7141248689141248690CG24GENIChomozygous69180454
7141249540141249541CT20GENIChomozygous69180455
7141250499141250500TC25GENIChomozygous69180456
7141250806141250807AG44GENIChomozygous69180457
7141250944141250945AG21GENIChomozygous69180458