chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168587733168587734AG27GENIChomozygous60936338
1168587803168587804CCGAAGAAGATGGAGGCA22GENIChomozygous60936340
1168587863168587864A-11GENIChomozygous60936342
1168588004168588005TG18GENIChomozygous60936343
1168588005168588006GA18GENIChomozygous60936344
1168588392168588393TC18GENIChomozygous60936345
1168588574168588576GG--1GENIChomozygous60936346
1168588735168588736CT22GENIChomozygous60936347
1168589165168589166GA21GENIChomozygous60936348
1168589285168589286GA22GENIChomozygous60936349
1168589370168589371AC19GENIChomozygous60936350
1168589404168589405CT19GENIChomozygous60936351
1168589557168589558TTG16GENIChomozygous60936352
1168589694168589695AT14GENIChomozygous60936353
1168589784168589785AG15GENIChomozygous60936354
1168589965168589966TC19GENIChomozygous60936355
1168590092168590093TC27GENIChomozygous60936356
1168590119168590120GC30GENIChomozygous60936357
1168590191168590192AT25GENIChomozygous60936358
1168590546168590547GA27GENIChomozygous60936359
1168590811168590812AG20GENIChomozygous60936360
1168591035168591036AG11GENIChomozygous60936361
1168591064168591065AG9GENIChomozygous60936362
1168591092168591093AG6GENIChomozygous60936363
1168591205168591206AAAC6GENICheterozygous60936364
1168591205168591206AAACACACACAC6GENICheterozygous62247649
1168591834168591835CT14GENIChomozygous60936365