chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181870484181870485GA18GENICheterozygous533144770
4181871086181871087TC25GENICpossibly homozygous533144771
4181871589181871590AG23GENICpossibly homozygous533144772
4181871907181871908CT32GENICpossibly homozygous536582206
4181872014181872015CT37GENIChomozygous536582207
4181872168181872169GT33GENICpossibly homozygous536582208
4181872359181872360TC10GENIChomozygous536582209
4181872420181872421A-1GENIChomozygous695519284
4181872427181872428A-1GENIChomozygous695519285
4181872443181872444A-2GENIChomozygous695519286