chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142514133142514134TC23GENIChomozygous144743382
5142514200142514201TG27GENIChomozygous144743383
5142514246142514247GA32GENIChomozygous144743384
5142514336142514337GT29GENIChomozygous144743385
5142514680142514681AG18GENIChomozygous144743386
5142514697142514698GC18GENIChomozygous144743387
5142519118142519119C12GENICpossibly homozygous137347004