chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86234510062345100G11GENIChomozygous130363420
86234527562345275T8GENIChomozygous131048818
86234721862347219TC9GENIChomozygous116836258
86234759562347596GT14GENIChomozygous116836260
86234760362347603A16GENIChomozygous131048819
86234815262348153TG23GENIChomozygous116836262
86234919362349194TC6GENIChomozygous116836264
86235003762350038GA15GENIChomozygous116836268
86235006762350068CT17GENIChomozygous116836270
86235514662355147CG8GENIChomozygous116836276
86235544562355446CT14GENIChomozygous116836278
86235602862356029TA12GENIChomozygous116836280
86235677362356774CT10GENIChomozygous116836282
86235694762356948CA16GENIChomozygous116836284
86235863162358632TC11GENIChomozygous116836286
86236014162360142GA20GENICpossibly homozygous116836288
86236047062360471CT14GENIChomozygous116836290
86236273762362738GA13GENIChomozygous116836292
86236352462363525CT18GENIChomozygous116836294
86236491362364914CG11GENIChomozygous116836300
86236503762365039AG9GENIChomozygous131048820
86236506962365070AG8GENIChomozygous116836302
86236586062365861AG9GENIChomozygous116836304
86236673662366737TC12GENIChomozygous116836306
86236798762367988CT10GENIChomozygous116836308
86236808562368086CT10GENIChomozygous116836310