chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461751986175199TG16GENICpossibly homozygous967822739
1461755176175518TC26GENIChomozygous967822740
1461767686176769AT20GENIChomozygous967822741
1461771496177150TC26GENIChomozygous967822742
1461774006177401GC24GENIChomozygous967822743
1461774566177457TC28GENICpossibly homozygous967822744
1461775596177560AG29GENICpossibly homozygous967822745
1461776266177627AG27GENICpossibly homozygous967822746
1461778266177827AG19GENIChomozygous967822747
1461811396181140GA16GENIChomozygous967822748
1462148646214865CT8GENIChomozygous967822749
1462166006216601CT12GENIChomozygous967822750
1462189296218930CT23GENIChomozygous967822751
1462189636218964CG27GENIChomozygous967822752
1462193116219312CT15GENIChomozygous967822753
1462194456219446GA23GENICpossibly homozygous967822754
1462196006219601GA36GENICpossibly homozygous967822755
1462202146220215CG18GENIChomozygous967822756
1462202236220224CT20GENIChomozygous967822757
1462204066220407GA12GENIChomozygous967822758
1462207146220715AG19GENIChomozygous967822759
1462209816220982AG21GENIChomozygous967822760
1462212306221231TC18GENIChomozygous967822761