chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142175419142175419GCCCA63GENIChomozygous127439697
1142176024142176025TC42GENIChomozygous108262808
1142176738142176739AG60GENIChomozygous108262810
1142176876142176876A32GENICpossibly homozygous127439698
1142177369142177370CT57GENIChomozygous108262812
1142181054142181055AG52GENIChomozygous108262814
1142181567142181568AG57GENIChomozygous108262816
1142182008142182009CG53GENIChomozygous108262818
1142182549142182550AG49GENIChomozygous108262820
1142183360142183361CT73GENIChomozygous108262822
1142183567142183568CT63GENIChomozygous108262824