chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18386581283865813TG39GENIChomozygous75044955
18386623183866232AG47GENIChomozygous75044957
18386627983866280AG39GENIChomozygous75044959
18386653083866531CT26GENIChomozygous74213268
18386664483866645AG32GENIChomozygous75044961
18386685083866851AC22GENIChomozygous75044963
18386715683867157GA20GENIChomozygous75044964
18386761383867614GA24GENIChomozygous75044966
18386762883867629CT27GENICpossibly homozygous75044968
18386817283868173GA43GENIChomozygous75044970
18386819983868200GA34GENIChomozygous75044972
18386850783868508TA32GENIChomozygous75044974
18386902083869021TC26GENIChomozygous75044979
18386905783869058AG22GENIChomozygous75044981
18387104483871045CT28GENIChomozygous75044983