chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2232904337232904338CT24GENIChomozygous75722666
2232904653232904654AG24GENIChomozygous74451029
2232905340232905341TC27GENIChomozygous74451033
2232912960232912961TA15GENIChomozygous75722670
2232913275232913276GT28GENIChomozygous74451047
2232913560232913561CG22GENICheterozygous74451049
2232913830232913831GA12GENICpossibly homozygous74451051
2232913582232913583CT25GENICheterozygous74941077
2232915457232915458GA29GENIChomozygous75722672
2232916048232916049AT26GENIChomozygous75722674
2232916908232916909CT9GENICheterozygous74941095
2232918789232918790AG21GENIChomozygous74451063
2232920161232920162TG23GENIChomozygous74451071
2232923096232923097TA16GENICheterozygous78681899
2232923092232923093TA17GENICheterozygous78717139
2232923094232923095TA18GENICheterozygous78717140
2232924072232924073CA22GENIChomozygous74451087