chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266257617266257618GA26GENIChomozygous957107932
1266259480266259481TG36GENIChomozygous957107933
1266259955266259956TC25GENIChomozygous957107934
1266260071266260072AC15GENIChomozygous957107935
1266260704266260705GA16GENIChomozygous957107936
1266260846266260847TA17GENIChomozygous957107937
1266261396266261397GC34GENIChomozygous957107938
1266262006266262007GC8GENIChomozygous957107939
1266262051266262052TC9GENIChomozygous957107940
1266262303266262304AG24GENIChomozygous957107941
1266262580266262581CT27GENIChomozygous957107942
1266263068266263069CA33GENIChomozygous957107943
1266264337266264338TA19GENIChomozygous957107944
1266264589266264590AG14GENIChomozygous957107945
1266265228266265229AG9GENIChomozygous957107946
1266266414266266415GT9GENIChomozygous957107947
1266266712266266713CT22GENIChomozygous957107948
1266267954266267955TC35GENIChomozygous957107949
1266268309266268310GA16GENIChomozygous957107950
1266270325266270326AG8GENIChomozygous957107951