chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265290448265290449GA18GENIChomozygous108636938
1265290481265290482CT21GENIChomozygous109027780
1265290684265290685AG32GENIChomozygous108636939
1265290865265290866TC25GENIChomozygous108636940
1265291139265291140GA27GENIChomozygous109377748
1265291237265291238TC25GENIChomozygous108636941
1265291484265291485TC24GENIChomozygous108636942
1265291873265291874TA29GENIChomozygous108636943
1265292526265292527GA35GENICpossibly homozygous109027782
1265293507265293508CT28GENIChomozygous108636944
1265294546265294547CT26GENICheterozygous109377750
1265296127265296128AG21GENIChomozygous108636947
1265298829265298830GA29GENIChomozygous109058207