chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141246476141246477TC30GENIChomozygous69180442
7141246502141246503CA28GENIChomozygous69180443
7141247268141247269CT31GENIChomozygous69180444
7141247856141247857GA43GENIChomozygous69180445
7141247891141247892TG40GENICpossibly homozygous69180446
7141248371141248372TA41GENIChomozygous69180447
7141248480141248481CA35GENIChomozygous69180448
7141249540141249541CT32GENIChomozygous69180455
7141250499141250500TC33GENIChomozygous69180456
7141250806141250807AG36GENIChomozygous69180457
7141250944141250945AG42GENIChomozygous69180458