chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2224957415224957416CCTT2GENIChomozygous59415456
2224958080224958081CT6GENICheterozygous59415461
2224958897224958898CT2GENIChomozygous59415463
2224960452224960453TC6GENIChomozygous59415466
2224962375224962376GA18GENICpossibly homozygous59415467
2224962936224962937TG14GENICpossibly homozygous59415468
2224963746224963747AAG3GENIChomozygous59415471
2224969020224969021AG10GENIChomozygous59415472
2224976399224976400TG7GENIChomozygous59415478
2224976562224976563TA3GENIChomozygous59415479
2224977718224977719AG26GENIChomozygous59415480
2224978449224978450TA10GENIChomozygous59415481
2224979629224979630GA9GENIChomozygous59415483