chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141246476141246477TC12GENIChomozygous69180442
7141246502141246503CA22GENIChomozygous69180443
7141247268141247269CT26GENIChomozygous69180444
7141247856141247857GA17GENIChomozygous69180445
7141247891141247892TG20GENIChomozygous69180446
7141248371141248372TA20GENIChomozygous69180447
7141248480141248481CA20GENIChomozygous69180448
7141249540141249541CT22GENIChomozygous69180455
7141250499141250500TC15GENICpossibly homozygous69180456
7141250806141250807AG25GENIChomozygous69180457
7141250944141250945AG20GENIChomozygous69180458