chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64070110940701110GC22GENIChomozygous947028364
64070290140702902GA22GENIChomozygous947028365
64070335840703359AG13GENIChomozygous947028366
64070400540704006TA24GENIChomozygous947028367
64070521840705219CT7GENIChomozygous947028368
64070531940705320GT10GENIChomozygous947028369
64070555740705558GA25GENIChomozygous947028370
64070567340705674AT21GENIChomozygous947028371
64070587140705872TA29GENIChomozygous947028372
64070612040706121AG20GENIChomozygous947028373
64070677240706773CT31GENICpossibly homozygous947028374
64070716540707166CT19GENIChomozygous947028375
64070747540707476GT15GENIChomozygous947028376
64070749640707497TG16GENIChomozygous947028377
64070799540707996GA15GENIChomozygous947028378
64070879140708792AG25GENIChomozygous947028379
64070914340709144TA34GENIChomozygous947028380
64070915340709154TG31GENIChomozygous947028381
64070988040709881GA31GENIChomozygous947028382
64070994140709942AG29GENIChomozygous947028383
64071013440710135GA28GENIChomozygous947028384
64071166440711665CG19GENIChomozygous947028385
64071331540713316TC18GENIChomozygous947028386
64071333840713339GA18GENIChomozygous947028387