chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168587733168587734AG32GENIChomozygous60936338
1168587803168587804CCGAAGAAGATGGAGGCA22GENIChomozygous60936340
1168587863168587864A-26GENICpossibly homozygous60936342
1168588004168588005TG26GENIChomozygous60936343
1168588005168588006GA26GENIChomozygous60936344
1168588392168588393TC19GENIChomozygous60936345
1168588735168588736CT19GENIChomozygous60936347
1168589165168589166GA28GENIChomozygous60936348
1168589285168589286GA24GENIChomozygous60936349
1168589370168589371AC27GENIChomozygous60936350
1168589404168589405CT25GENIChomozygous60936351
1168589557168589558TTG26GENIChomozygous60936352
1168589694168589695AT30GENIChomozygous60936353
1168589784168589785AG24GENIChomozygous60936354
1168589965168589966TC32GENIChomozygous60936355
1168590092168590093TC25GENIChomozygous60936356
1168590119168590120GC29GENIChomozygous60936357
1168590191168590192AT25GENIChomozygous60936358
1168590546168590547GA29GENIChomozygous60936359
1168590811168590812AG29GENIChomozygous60936360
1168591035168591036AG23GENIChomozygous60936361
1168591064168591065AG18GENIChomozygous60936362
1168591092168591093AG22GENIChomozygous60936363
1168591205168591206AAAC4GENICheterozygous60936364
1168591834168591835CT32GENIChomozygous60936365