chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37755116677551167CT9GENIChomozygous613151148
37755588777555888CG28GENIChomozygous613151149
37755717277557173GA33GENIChomozygous613151150
37755796177557962A-25GENIChomozygous737103386
37755796977557970A-26GENIChomozygous737103387
37755805177558052GA27GENIChomozygous613151151
37755809777558098GT29GENIChomozygous615318898
37755829077558291G-21GENIChomozygous737103388
37755854577558546GA46GENIChomozygous613151152
37756013477560135GA33GENIChomozygous613151153
37756034777560348TC32GENIChomozygous615318899
37756062277560624TA--29GENIChomozygous737103389
37756163877561639CA27GENIChomozygous613151154
37756245777562458AG36GENIChomozygous613151155
37756310377563104TA22GENICpossibly homozygous613151156
37756310477563105TA21GENICpossibly homozygous613151157
37756409077564091AT30GENIChomozygous615318900
37756494777564948AAT13GENICheterozygous737103392
37756554577565546G-28GENIChomozygous737103393
37756570477565705GGT7GENICpossibly homozygous737103394
37756570577565706GGT7GENICpossibly homozygous737103395
37756735477567355T-10GENIChomozygous737103397
37756883477568835AG40GENIChomozygous613151158
37756906377569065AA--29GENIChomozygous737103400
37756915977569160AG26GENIChomozygous613151159
37756919877569213ATACCACTAGGGTCT---------------13GENIChomozygous737103401
37756952977569530GA29GENIChomozygous613151160
37756960777569608GA29GENIChomozygous613151161