chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117025942117025943AT59GENICpossibly homozygous115846105
7117025945117025946AT61GENICpossibly homozygous115846107
7117027454117027455GA45GENICheterozygous115846109
7117027919117027920GA32GENIChomozygous116393555
7117028396117028397AG43GENIChomozygous115846111
7117028428117028429CA40GENIChomozygous115846113
7117028918117028919CG56GENIChomozygous115846115
7117029050117029051AG62GENICheterozygous115846117
7117031833117031834AG53GENIChomozygous115846119
7117032484117032485TC50GENICheterozygous115846121
7117029674117029675AG55GENICheterozygous116224748
7117029786117029787CA60GENICheterozygous116224749
7117029813117029814CT62GENICheterozygous128562327
7117029845117029846TG64GENICheterozygous128562328
7117030720117030720AAGATATTCCCAGGGTTGGGGATTTAGCTCAGTGGTAGAGCAGTTGCCTAGG19GENIChomozygous128510423
7117032498117032500CT45GENICheterozygous128510424
7117032066117032067AG33GENIChomozygous131440344
7117032067117032068AT33GENIChomozygous131440345
7117032582117032583AG24GENIChomozygous115846123
7117032865117032866TC38GENICheterozygous128562329