chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263913989263913990AG40GENIChomozygous108634368
1263914210263914211TC50GENIChomozygous108634370
1263914932263914933CT50GENIChomozygous108634372
1263917069263917070CT27GENIChomozygous108634374
1263917124263917125TC30GENICheterozygous108634376
1263917161263917162CT24GENICheterozygous108634378
1263917165263917166CT25GENICheterozygous108634379
1263917246263917247AG25GENIChomozygous108634381
1263917407263917408AC37GENIChomozygous108634383
1263917534263917535AC39GENIChomozygous108634385
1263918066263918067GA28GENIChomozygous108634387
1263919098263919099TC52GENIChomozygous108634388
1263919321263919322CT30GENIChomozygous108634390
1263919732263919733GA48GENIChomozygous108634392
1263919763263919764CT46GENIChomozygous108634394
1263919802263919803CT44GENIChomozygous108634396
1263919877263919878TC40GENIChomozygous108634397
1263920743263920744AG51GENIChomozygous108634399