chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15779421257794213TG30GENIChomozygous934003294
15779574457795745TC26GENIChomozygous934003295
15779591657795917CT28GENIChomozygous934003296
15779770657797707AG29GENIChomozygous934003297
15779934557799346CT21GENIChomozygous934003298
15779989457799895GA31GENIChomozygous934003299
15780045857800459TC35GENIChomozygous934003300
15780096457800965GA25GENIChomozygous934003301
15780102657801027CT23GENIChomozygous934003302
15780128157801282GA36GENIChomozygous934003303
15780273957802740GC27GENIChomozygous934003304
15780296957802970TC31GENIChomozygous934003305
15780299057802991CT31GENIChomozygous934003306
15780344257803443TA27GENIChomozygous934003307
15780356157803562TA40GENICpossibly homozygous934003308
15780783257807833GA23GENICheterozygous934003309
15780813357808134AG10GENIChomozygous934003310
15780824057808241TA19GENIChomozygous934003311
15780833457808335TC16GENIChomozygous934003312
15780839757808398TC13GENIChomozygous934003313
15780866357808664AG28GENIChomozygous934003314
15780868657808687GA27GENIChomozygous934003315
15780884057808841AG24GENIChomozygous934003316
15780898457808985AG26GENIChomozygous934003317
15780899457808995GA25GENIChomozygous934003318
15781073657810737GA17GENIChomozygous934003319
15781326557813266AT24GENIChomozygous934003320
15781465457814655AC8GENIChomozygous934003321
15781551557815516AC10GENIChomozygous934003322
15781552957815530CT7GENIChomozygous934003323
15781649857816499CG31GENIChomozygous934003324
15781678257816783CT38GENIChomozygous934003325
15781701057817011TA39GENICpossibly homozygous934003326
15781766557817666TC28GENIChomozygous934003327
15781792857817929TC26GENIChomozygous934003328
15781851957818520AG18GENIChomozygous934003329
15781900157819002CT26GENIChomozygous934003330
15781903257819033CA32GENIChomozygous934003331