chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108804690988046910TC28GENIChomozygous116672235
108804728888047289TG60GENIChomozygous116672237
108804730088047301CT61GENIChomozygous116672239
108804730688047307GA63GENIChomozygous116672241
108804732088047321AG67GENIChomozygous116672243
108804733688047337TC73GENIChomozygous116672245
108804735588047356CT72GENIChomozygous116672247
108804737188047372CA64GENICpossibly homozygous116672249
108804738688047387TC59GENIChomozygous116672251
108804739588047396CA56GENIChomozygous116672253
108804743088047431CA54GENICpossibly homozygous116672255
108804744688047447CT50GENICpossibly homozygous116672257
108804789588047896AG63GENIChomozygous116672259
108804800388048004GA73GENIChomozygous116672261
108804808788048088GA58GENIChomozygous116672263
108804815288048153AG43GENIChomozygous116672265
108804819588048196TC41GENIChomozygous116672267
108804825288048253AC39GENIChomozygous116672269
108804832288048323AC47GENIChomozygous116672271
108804838588048386GA43GENICpossibly homozygous116672273
108804865588048656TA51GENIChomozygous116672275
108804904088049041CG69GENIChomozygous116672277
108804942988049430GA41GENIChomozygous116672279
108804956988049570AC45GENIChomozygous116672281
108804990688049907GA33GENIChomozygous116672283
108805022788050228GA43GENIChomozygous116672285
108805043488050435TC34GENIChomozygous116672287