chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101452960114529602AT41GENIChomozygous116496633
101452977714529778CT56GENIChomozygous116496635
101453100014531001AG7GENICpossibly homozygous117982422
101453100414531005AG9GENICheterozygous117982424
101453100814531009AG10GENICheterozygous117982426
101453101214531013AG10GENICpossibly homozygous117982428
101453101614531017AG10GENICpossibly homozygous117982430
101453103214531033AG12GENICpossibly homozygous117982432
101453103614531037GA12GENICpossibly homozygous117982433
101453157314531574TG46GENIChomozygous116496637