chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5171656438171656439GA11GENIChomozygous56195175
5171656452171656453GA6GENIChomozygous56195176
5171657088171657089CT18GENIChomozygous56195177
5171657737171657738CG28GENICpossibly homozygous55839873
5171657995171657996CT24GENICpossibly homozygous55839874
5171658091171658092TG21GENICpossibly homozygous55839875
5171658539171658540GC15GENICpossibly homozygous55839876
5171658736171658737TG22GENIChomozygous55839877
5171658883171658884CT37GENIChomozygous56195179
5171659005171659006CCT11GENIChomozygous55839878
5171659550171659551GA18GENIChomozygous56195180
5171659820171659821TC17GENICpossibly homozygous55839879
5171659883171659884TG32GENIChomozygous55839881
5171660011171660012TC19GENICpossibly homozygous55839882
5171660376171660377GA16GENIChomozygous56195181
5171660423171660424TC14GENIChomozygous55839883
5171660841171660842CT27GENIChomozygous56195182