chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
49918720199187202AT21GENICpossibly homozygous957789516
49918760499187605CT14GENIChomozygous957789517
49918790199187902GA13GENIChomozygous957789518
49918814299188143TA17GENIChomozygous957789519
49918823799188238CG26GENIChomozygous957789520
49919509299195093GA22GENIChomozygous957789521
49919549099195491AG20GENIChomozygous957789522
49919579199195792GA23GENIChomozygous957789523
49919861099198611TC20GENIChomozygous957789524
49919917399199174CA25GENIChomozygous957789525
49919955499199555AG3GENIChomozygous957789526
49920083399200834TC29GENIChomozygous957789527