chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2035580803558081TC31GENIChomozygous109069062
2035585903558591CT35GENIChomozygous109231767
2035598083559809GA28GENIChomozygous109231768
2035604273560428AT12GENICheterozygous109069066
2035604283560429AG12GENICheterozygous109294484
2035604573560458AG12GENIChomozygous109462990
2035609643560965GC19GENICpossibly homozygous119844353
2035613913561392AG27GENIChomozygous109069070
2035619163561917TG21GENIChomozygous109231769
2035629953562996CT4GENIChomozygous119844354
2035632393563240TA17GENIChomozygous109231770
2035659173565918CT27GENIChomozygous109231771
2035723283572329GT35GENIChomozygous109231772
2035736473573648GA25GENIChomozygous109069095
2035738293573830GA23GENIChomozygous109370796