chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2232904337232904338CT19GENIChomozygous75722666
2232904653232904654AG37GENICpossibly homozygous74451029
2232905340232905341TC29GENIChomozygous74451033
2232912960232912961TA9GENIChomozygous75722670
2232913275232913276GT23GENIChomozygous74451047
2232913830232913831GA23GENIChomozygous74451051
2232915457232915458GA23GENIChomozygous75722672
2232916048232916049AT22GENIChomozygous75722674
2232918789232918790AG18GENIChomozygous74451063
2232920161232920162TG28GENIChomozygous74451071
2232923100232923101TA22GENICheterozygous78681901
2232923096232923097TA22GENICheterozygous78681899
2232923098232923099TA21GENICheterozygous78681900
2232923092232923093TA22GENICheterozygous78717139
2232923094232923095TA22GENICheterozygous78717140
2232923102232923103TA21GENICheterozygous78681902
2232924072232924073CA28GENIChomozygous74451087