chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37206221572062216CA69GENIChomozygous806845742
37206255872062559GA50GENIChomozygous806845743
37206372472063725AG35GENIChomozygous806845744
37206425472064255AG49GENIChomozygous806845745
37206460372064604CT65GENIChomozygous806845746
37206494472064945CA63GENICpossibly homozygous806845747
37206638972066390AG56GENIChomozygous806845748
37206679972066800CG62GENIChomozygous806845749
37206720772067208CT55GENIChomozygous806845750
37206726272067263CT49GENICpossibly homozygous806845751
37206733372067334CT38GENICpossibly homozygous806845752
37206734572067346GT32GENICpossibly homozygous806845753
37206735272067353AG28GENICpossibly homozygous806845754
37206743872067439GA24GENIChomozygous806845755
37206747872067479CT35GENIChomozygous806845756
37206765072067651GA42GENIChomozygous806845757
37206824472068245AG54GENIChomozygous806845758
37206827772068278AG51GENIChomozygous806845759
37206839472068395TC51GENIChomozygous806845760
37206998972069990GC32GENIChomozygous806845761
37207007172070072GA56GENIChomozygous806845762
37207046172070462CT48GENICpossibly homozygous806845763