chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144056342144056343GA19GENIChomozygous114036416
5144056493144056494CT20GENICpossibly homozygous114036417
5144056778144056779CA30GENIChomozygous114036418
5144057053144057054GA23GENIChomozygous114036419
5144057780144057781CT31GENIChomozygous114036420
5144057969144057970TA28GENIChomozygous114036421
5144058064144058065CT32GENIChomozygous114036422
5144058606144058607AC20GENIChomozygous114036423
5144060166144060167TA30GENIChomozygous114036424
5144061875144061876AT12GENIChomozygous114036425
5144063376144063377CT22GENIChomozygous114036426
5144064054144064055GA31GENIChomozygous114036427
5144064561144064562TC22GENIChomozygous114036428
5144064794144064795AG32GENICpossibly homozygous114036429
5144064944144064945TC24GENICpossibly homozygous114036430