chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261338174261338175AC63GENIChomozygous108629357
1261339472261339473AT55GENICpossibly homozygous108629358
1261341260261341261AG64GENIChomozygous108629361
1261344363261344364AC45GENIChomozygous108629365
1261343259261343260CA53GENIChomozygous134397132
1261354795261354796AG58GENIChomozygous109026004
1261354814261354815AG60GENIChomozygous108629380
1261354836261354837AT56GENIChomozygous109026006
1261356892261356893AG47GENIChomozygous108629386
1261340228261340229A60GENIChomozygous134390668
1261342070261342070TT58GENIChomozygous134390669
1261343628261343629A44GENIChomozygous131267478
1261344638261344660AGGGCCTTGCGCTTGCTAGGCA12GENIChomozygous134390670
1261344591261344591T9GENICheterozygous131267479
1261352804261352804TGT16GENICheterozygous134390671
1261355217261355218T44GENIChomozygous134390672
1261362204261362204T45GENICpossibly homozygous127507129