chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461749166174917GT23GENIChomozygous970765756
1461753876175388AG18GENIChomozygous970765757
1461753886175389GA18GENIChomozygous970765758
1461767686176769AT20GENIChomozygous970765759
1461771496177150TC21GENIChomozygous970765760
1461774006177401GC14GENIChomozygous970765761
1461774566177457TC26GENIChomozygous970765762
1461775596177560AG21GENIChomozygous970765763
1461776266177627AG13GENIChomozygous970765764
1462166006216601CT27GENIChomozygous970765765
1462189296218930CT26GENIChomozygous970765766
1462189636218964CG34GENIChomozygous970765767
1462193116219312CT30GENIChomozygous970765768
1462194456219446GA35GENIChomozygous970765769
1462196006219601GA6GENIChomozygous970765770
1462202146220215CG14GENIChomozygous970765771
1462202236220224CT18GENIChomozygous970765772
1462204066220407GA12GENIChomozygous970765773
1462207146220715AG13GENIChomozygous970765774
1462207476220748TC13GENIChomozygous970765775
1462209816220982AG15GENIChomozygous970765776
1462212306221231TC16GENIChomozygous970765777