chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117649780117649781GA22GENIChomozygous57620989
3117649807117649808TC18GENICpossibly homozygous57620991
3117650938117650939CT22GENIChomozygous57620997
3117651440117651441AG14GENIChomozygous57621001
3117651465117651466CT14GENIChomozygous57621003
3117651549117651550AG6GENICheterozygous57621005
3117651656117651657TC5GENIChomozygous57621007
3117652153117652154GA10GENIChomozygous57621011
3117652307117652309AA--2GENIChomozygous57621013
3117652739117652740CT15GENICpossibly homozygous57621015
3117652796117652797GA15GENIChomozygous57621017
3117654405117654406GT8GENIChomozygous57621019
3117656167117656168CT13GENICpossibly homozygous57621021
3117656856117656858GT--12GENICheterozygous57621033
3117656935117656936GT21GENIChomozygous57621035
3117657290117657291GA18GENIChomozygous57621043
3117657301117657302CT14GENIChomozygous57621045
3117657351117657352CT13GENIChomozygous58691853
3117657352117657353GC13GENIChomozygous57621047
3117657569117657570GT21GENIChomozygous57621049
3117657798117657799CT14GENIChomozygous57621051
3117658335117658336GT30GENIChomozygous57621053
3117658793117658794CA40GENIChomozygous57621055