chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204754536204754537GA8GENIChomozygous62301537
1204754838204754839CG10GENICpossibly homozygous61063232
1204754967204754968AG3GENIChomozygous62301538
1204755226204755227AC5GENIChomozygous61063233
1204755365204755366TTG9GENIChomozygous62301539
1204755495204755496AT20GENIChomozygous61063234
1204758773204758774AACGTCCCAT6GENIChomozygous61063240
1204759225204759226TA11GENIChomozygous61063242
1204759233204759234TC11GENIChomozygous61063243
1204759320204759321TG30GENIChomozygous61063244