chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117025942117025943AT15GENIChomozygous115846105
7117025945117025946AT16GENIChomozygous115846107
7117027454117027455GA15GENICheterozygous115846109
7117027919117027920GA17GENIChomozygous116393555
7117028396117028397AG12GENIChomozygous115846111
7117028428117028429CA19GENIChomozygous115846113
7117028918117028919CG21GENIChomozygous115846115
7117029050117029051AG32GENICheterozygous115846117
7117031833117031834AG19GENIChomozygous115846119
7117032484117032485TC12GENICheterozygous115846121
7117029674117029675AG24GENICheterozygous116224748
7117029786117029787CA27GENICheterozygous116224749
7117029813117029814CT29GENICheterozygous128562327
7117029845117029846TG24GENICheterozygous128562328
7117030720117030720AAGATATTCCCAGGGTTGGGGATTTAGCTCAGTGGTAGAGCAGTTGCCTAGG8GENICpossibly homozygous128510423
7117032498117032500CT12GENICheterozygous128510424
7117032066117032067AG14GENIChomozygous131440344
7117032067117032068AT14GENIChomozygous131440345
7117032582117032583AG6GENIChomozygous115846123