chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2224957415224957416CCTT4GENICheterozygous59415456
2224958080224958081CT9GENIChomozygous59415461
2224958897224958898CT3GENICheterozygous59415463
2224960452224960453TC12GENIChomozygous59415466
2224962375224962376GA12GENICheterozygous59415467
2224962936224962937TG19GENICpossibly homozygous59415468
2224963178224963179AAT4GENICheterozygous59415469
2224963746224963747AAG1GENIChomozygous59415471
2224969020224969021AG6GENICheterozygous59415472
2224976399224976400TG12GENICheterozygous59415478
2224976562224976563TA8GENICheterozygous59415479
2224977718224977719AG12GENIChomozygous59415480
2224978449224978450TA19GENICpossibly homozygous59415481
2224979629224979630GA12GENIChomozygous59415483