chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72903015529030156AG9GENIChomozygous116131427
72903115929031160TC20GENIChomozygous116131429
72903252629032526A16GENICpossibly homozygous132652399
72903273729032737T20GENICpossibly homozygous132652400
72903275729032757TTG13GENIChomozygous132652401
72903435929034373GTGTGTGTGTGTTG7GENICheterozygous132652402
72903499629034999AGA15GENIChomozygous132652403
72903613629036137AT15GENIChomozygous116131431
72903622029036221TC23GENIChomozygous116131433
72903648429036485CG18GENIChomozygous116131435
72903881829038819TG17GENIChomozygous116131437
72903905329039056TGA16GENIChomozygous132652404
72903952629039526G12GENIChomozygous132652405
72904139229041393AC29GENIChomozygous116131439
72904148029041481GA26GENIChomozygous116131441
72904288629042887TC19GENIChomozygous116131443
72904290129042902AG20GENIChomozygous116131445
72904323529043235TTT17GENIChomozygous132652406