chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108910421989104220GA44GENIChomozygous116675074
108910513489105135GA48GENIChomozygous116675076
108910695589106956CT44GENIChomozygous116950482
108910769089107691TA47GENIChomozygous116675078
108910793289107933GA40GENIChomozygous116675080
108910973989109740TC39GENICpossibly homozygous116675082
108911308989113090GA25GENIChomozygous116675084
108911433289114333AC37GENIChomozygous116675086
108911456089114561AG42GENIChomozygous116675088
108911521289115213TC62GENIChomozygous116675090
108911550189115502CT48GENIChomozygous116675092
108911580189115802AG34GENIChomozygous116675094
108911693789116938CT40GENIChomozygous116675096
108911694989116950AG42GENIChomozygous116675098
108911733789117341TTTG29GENIChomozygous128843615
108910708189107084TTG32GENIChomozygous128843610
108911085989110859T51GENIChomozygous128843612
108911565189115651G39GENIChomozygous128843613
108911276489112765AT2GENICheterozygous118007484
108911630789116308CT11GENIChomozygous118007485
108911881489118815TG18GENIChomozygous118007486
108911947289119473TA49GENIChomozygous116950484
108912036289120362CC34GENIChomozygous128843616
108912051489120521CACACAC15GENICheterozygous132147102
108911885689118857AG25GENIChomozygous117197721
108912041689120417CA30GENIChomozygous116950486
108912582089125821TC34GENIChomozygous116675110