chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105622443356224434TC22GENIChomozygous117011556
105622576956225770A22GENICpossibly homozygous128819184
105622630156226301T8GENICheterozygous128819185
105622671856226719TC16GENIChomozygous116783296
105622922856229229CT7GENICheterozygous131101407
105622923156229232CT7GENICheterozygous131101408
105622924456229245GT6GENICheterozygous132883059
105623064756230647A15GENIChomozygous131094454
105623101956231020T20GENIChomozygous131094455
105623137856231379AG15GENIChomozygous116783298
105623387256233873CT25GENIChomozygous116783300
105623487556234875AAC11GENIChomozygous131094456
105623489556234896TC11GENIChomozygous116783302
105623553656235537AG27GENIChomozygous116783306
105623617856236178A11GENICheterozygous133423926
105623701856237019T22GENIChomozygous131094457
105623489856234899TC11GENIChomozygous117059647
105623207356232074CT34GENIChomozygous117059645