chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG5GENIChomozygous948976293
1266867306266867307GA15GENIChomozygous948976294
1266869171266869172TC24GENIChomozygous948976295
1266869354266869355CT19GENIChomozygous948976296
1266871195266871196CT7GENIChomozygous948976297
1266871799266871800AG28GENIChomozygous948976298
1266872295266872296GA6GENIChomozygous948976299
1266876378266876379AG14GENIChomozygous948976300
1266876812266876813GA15GENIChomozygous948976301
1266878355266878356CT20GENIChomozygous948976302
1266879795266879796TG9GENIChomozygous948976303
1266879804266879805AG8GENIChomozygous948976304
1266881234266881235CT15GENIChomozygous948976305
1266881721266881722AG10GENIChomozygous948976306
1266882385266882386GC16GENIChomozygous948976307
1266885292266885293AC9GENIChomozygous948976308
1266885604266885605GA12GENIChomozygous948976309
1266888529266888530CT17GENIChomozygous948976310
1266889651266889652TC19GENIChomozygous948976311
1266890046266890047TC11GENIChomozygous948976312
1266892512266892513TC13GENIChomozygous948976313
1266894775266894776GA18GENIChomozygous948976314
1266895476266895477AG16GENIChomozygous948976315
1266896747266896748TG13GENIChomozygous948976316
1266897388266897389TC10GENIChomozygous948976317
1266897506266897507GA10GENIChomozygous948976318
1266898357266898358AG23GENIChomozygous948976319
1266898962266898963GA13GENIChomozygous948976320
1266899513266899514GA13GENIChomozygous948976321
1266907705266907706AT14GENIChomozygous948976322