chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4232665984232665988GTGT----1GENIChomozygous692272531
4232671250232671251T-10GENICheterozygous692272532
4232699096232699098TG--14GENICheterozygous692272534
4232712797232712798CCAA16GENIChomozygous692272535
4232712799232712800CCGGACTTTTATTTAA8GENICpossibly homozygous692272536
4232725449232725450G-7GENIChomozygous692272537
4232725452232725453A-7GENIChomozygous692272538
4232725454232725455AT7GENIChomozygous527827395
4232725455232725456GGTC7GENIChomozygous692272539
4232727292232727293T-11GENICheterozygous692272540
4232728011232728012A-15GENICheterozygous692272541
4232728011232728012AAC15GENICpossibly homozygous692272542
4232728013232728014T-12GENICheterozygous692272544
4232747081232747082AG25GENIChomozygous527827396