chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2225552109225552110AG6GENIChomozygous110910941
2225552330225552331GA7GENIChomozygous110910942
2225552734225552735GC10GENIChomozygous110910943
2225557572225557573CG20GENIChomozygous110910944
2225559916225559917CT35GENIChomozygous110910945
2225561676225561677TC14GENICpossibly homozygous110271844
2225562004225562005CT19GENIChomozygous110910946
2225562165225562166GA15GENIChomozygous110910947
2225563222225563223GC24GENIChomozygous110910948
2225572959225572960GA30GENIChomozygous110910949
2225576134225576135CT23GENIChomozygous110910950
2225578540225578541CT5GENIChomozygous110910951
2225585522225585523CT35GENIChomozygous110910952
2225591683225591684GT5GENIChomozygous110271864
2225591687225591688AC5GENIChomozygous110626962
2225591691225591692AT4GENIChomozygous110626966
2225596746225596747TC15GENIChomozygous110271878
2225602709225602710AG34GENIChomozygous110910953
2225602769225602770AG27GENIChomozygous110910954
2225603490225603491TC22GENIChomozygous110271882
2225608042225608043GA47GENIChomozygous110910955
2225610562225610563TA22GENIChomozygous110910956
2225611115225611116AG29GENIChomozygous110271886