chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
156072251560722516CT14GENIChomozygous933389413
156072300660723007TG5GENIChomozygous933389414
156072339460723395TA11GENIChomozygous933389415
156072354960723550CA16GENIChomozygous933389416
156072355260723553CT16GENIChomozygous933389417
156072358960723590CT12GENIChomozygous933389418
156072359460723595GC10GENIChomozygous933389419
156072404160724042TG8GENIChomozygous933389420
156072406660724067AG6GENIChomozygous933389421
156072410360724104TC12GENIChomozygous933389422
156072411160724112AC13GENIChomozygous933389423
156072503060725031GA14GENIChomozygous933389424
156072557560725576TC5GENIChomozygous933389425
156073234660732347TC14GENIChomozygous933389426
156073477660734777TA7GENIChomozygous933389427
156073758560737586CA6GENIChomozygous933389428
156073856260738563CT12GENIChomozygous933389429
156073873060738731CT11GENIChomozygous933389430
156073906260739063GA3GENIChomozygous933389431
156074018560740186TA9GENIChomozygous933389432
156074745360747454AG9GENIChomozygous933389433
156074907160749072GT8GENIChomozygous933389434
156074908060749081GA6GENIChomozygous933389435
156074943760749438AG10GENIChomozygous933389436
156074954560749546CA9GENIChomozygous933389437
156074995560749956CA8GENIChomozygous933389438
156075067960750680AG14GENIChomozygous933389439
156075069760750698GA12GENIChomozygous933389440
156075076960750770AC13GENIChomozygous933389441
156075079060750791TC11GENIChomozygous933389442
156075112060751121GA7GENIChomozygous933389443
156075556960755570TG8GENIChomozygous933389444
156075599360755994AG7GENIChomozygous933389445
156075847360758474GT14GENIChomozygous933389446
156076161960761620TG13GENIChomozygous933389447
156076164660761647GA11GENIChomozygous933389448
156076470160764702GA10GENIChomozygous933389449