chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2192776272192776273AT25GENICpossibly homozygous974994014
2192776517192776518CT25GENIChomozygous974994015
2192776744192776745GA24GENIChomozygous974994016
2192777001192777002CT23GENIChomozygous974994017
2192777850192777851CT26GENIChomozygous974994018
2192777875192777876GA27GENIChomozygous974994019
2192777929192777930GA28GENIChomozygous974994020
2192779858192779859CT27GENIChomozygous974994021
2192780076192780077TC33GENIChomozygous974994022
2192780258192780259CT26GENIChomozygous974994023
2192780313192780314CG34GENIChomozygous974994024