chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104631490846314909TC34GENIChomozygous116772488
104631592546315926GA26GENIChomozygous116772490
104631593046315931TG28GENIChomozygous116772492
104631616346316164GT33GENIChomozygous116877695
104631725746317258TC22GENIChomozygous116772494
104631761046317611AG18GENIChomozygous116877697
104631784046317841GA15GENIChomozygous116772496
104631881946318820CA19GENIChomozygous116772498
104631925046319251AG28GENIChomozygous116772500
104631971646319717AG40GENIChomozygous116772502
104631973846319739AC41GENIChomozygous116772504
104631975246319753CA40GENICheterozygous116772506
104631988646319887GA34GENIChomozygous116772508
104632012546320126GA23GENIChomozygous116772510
104632076046320761AG18GENIChomozygous116772512
104632184446321845CT21GENIChomozygous116772514
104632331246323313TC15GENIChomozygous116772516
104632345246323453TC23GENIChomozygous116772518
104632411546324116CT37GENIChomozygous116877699
104632433246324333CT33GENIChomozygous116772526
104632445546324456AG26GENIChomozygous116772528
104632468446324685CG25GENIChomozygous116772530
104632562646325627CT27GENIChomozygous116877701
104632681346326814GC19GENIChomozygous116772532
104632713946327140GA38GENIChomozygous116772534
104632718246327183AG32GENIChomozygous116772536
104632724246327243GA24GENIChomozygous116772538
104632749846327499AG20GENIChomozygous116772540
104632761646327617TG16GENIChomozygous116585675
104631976646319767CA46GENICheterozygous118102769
104631978046319781AC46GENICheterozygous118102771
104632417646324177TC29GENIChomozygous116585671
104632851746328518CT23GENIChomozygous116772542
104632915546329156GT29GENIChomozygous116877703
104632928246329283CT24GENIChomozygous116772544