chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224978299224978300TC35GENICpossibly homozygous108556327
1224981533224981534CT41GENIChomozygous108556328
1224981714224981715CT44GENIChomozygous108556329
1224981897224981898CA34GENIChomozygous108556330
1224982809224982810CT37GENIChomozygous108556331
1224982985224982986CT32GENIChomozygous108556332
1224983154224983155AG36GENIChomozygous108556333