chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1176728294176728295GA16GENIChomozygous143800663
1176728694176728695CT16GENIChomozygous143800664
1176728872176728873TC20GENIChomozygous135755145
1176728937176728940GTG16GENIChomozygous135446869
1176729393176729394TC22GENIChomozygous135755146
1176729829176729830CT14GENIChomozygous135755147
1176730938176730939CT20GENIChomozygous143800665
1176733015176733016TC22GENIChomozygous135755149
1176734062176734063GT13GENIChomozygous143800666
1176734480176734481GC16GENIChomozygous135755150
1176735428176735429GA13GENIChomozygous135755152
1176735816176735817CT11GENIChomozygous135755153
1176737813176737813A12GENIChomozygous135446873
1176738342176738343GT20GENICpossibly homozygous143800667
1176739144176739145GA11GENIChomozygous135755156
1176739145176739146AC11GENIChomozygous135755157
1176739877176739878GA6GENIChomozygous143800668
1176740375176740376AG8GENIChomozygous135755159
1176740521176740522A5GENICheterozygous402974279
1176738676176738677AT6GENICheterozygous153901725
1176738676176738677AG6GENICheterozygous403701558
1176740519176740520A5GENICheterozygous402974277
1176740519176740520AG5GENICheterozygous402974278
1176741611176741612CT21GENIChomozygous143800669
1176741885176741886AC17GENIChomozygous135755161
1176742256176742257TC15GENIChomozygous135755162
1176742311176742312AG13GENIChomozygous135755163
1176742537176742538AT9GENIChomozygous135755164
1176742556176742557CT7GENIChomozygous143800670
1176740521176740522AG5GENICheterozygous402974280
1176740523176740524A5GENICheterozygous402974281
1176740523176740524AG5GENICheterozygous402974282