chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1192933425192933426GC34GENIChomozygous108469312
1192934969192934970CT66GENIChomozygous108469313
1192936008192936009CT58GENICpossibly homozygous108469314
1192936683192936684GT26GENIChomozygous108469315
1192937971192937972TC64GENIChomozygous108469316
1192939379192939380CT32GENICpossibly homozygous108469317
1192940570192940571AG46GENIChomozygous108469318
1192940615192940616TC37GENIChomozygous108469319
1192940616192940617TC37GENICpossibly homozygous108469320
1192941118192941119AG40GENIChomozygous108469321
1192942177192942178AT52GENIChomozygous108469322
1192942247192942248TC47GENIChomozygous108469323
1192942598192942599CA47GENICpossibly homozygous108469324
1192944597192944598GA27GENIChomozygous108469325
1192946694192946695TC50GENIChomozygous108469326
1192946946192946947CT46GENIChomozygous108469327
1192948177192948178CT40GENIChomozygous108469328
1192948323192948324GA64GENIChomozygous108469329
1192948455192948456CA62GENIChomozygous108469330
1192949150192949151CG47GENIChomozygous108469331
1192949847192949848GT46GENIChomozygous108469332
1192949848192949849GT45GENIChomozygous108469333
1192956781192956782TG42GENIChomozygous108469334
1192961036192961037GA62GENIChomozygous108469335
1192963040192963041TC29GENIChomozygous108469336