chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213607013213607014GC11GENIChomozygous108531622
1213607826213607827AC24GENIChomozygous108990016
1213607901213607902AT18GENIChomozygous108531623
1213608582213608583TC24GENIChomozygous108531624
1213608640213608641TC31GENIChomozygous108531625
1213608735213608736GA21GENIChomozygous108531626
1213608765213608766GA25GENIChomozygous108990017
1213611065213611066GT12GENIChomozygous108531627
1213611205213611206TA6GENICheterozygous108531628
1213611207213611208GA6GENICheterozygous108531629
1213611241213611242GA12GENICpossibly homozygous108990018
1213611980213611981GC29GENIChomozygous108531630
1213612782213612783AC29GENIChomozygous108531631