chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126348130126348131AG20GENIChomozygous119016699
5126349713126349714TC28GENIChomozygous113997472
5126349986126349987TC26GENIChomozygous113997478
5126350097126350098CT17GENIChomozygous113997486
5126351184126351185CT26GENIChomozygous119016700
5126351573126351574AG30GENIChomozygous113997526
5126352263126352264AG16GENIChomozygous113997534
5126352947126352948AG29GENIChomozygous113997554
5126353068126353069TG32GENIChomozygous113997556
5126353860126353861AG26GENIChomozygous113997562
5126356156126356157TC22GENIChomozygous119016701
5126358811126358812CG14GENIChomozygous119016702
5126359101126359102AG20GENIChomozygous113997592
5126359835126359836AT12GENIChomozygous119016703
5126361839126361840TC6GENIChomozygous119016704
5126361843126361844AC6GENIChomozygous118845359
5126363534126363535CT28GENIChomozygous119016705
5126363584126363585TG32GENIChomozygous119016706
5126367162126367163AG27GENIChomozygous119016707
5126368803126368804CT15GENIChomozygous119016708
5126369296126369297CT17GENIChomozygous119016709
5126372512126372513AG19GENIChomozygous119016710
5126372993126372994GA26GENIChomozygous113997637
5126373623126373624GA26GENIChomozygous119016711
5126384781126384782TG10GENIChomozygous113997665
5126385159126385160GA21GENIChomozygous119016712
5126390574126390575GA21GENIChomozygous119016713
5126391658126391659GA26GENIChomozygous119016714
5126393606126393607AG28GENIChomozygous113997728