chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4164938157164938158CA18GENIChomozygous58867593
4164938239164938240AG18GENIChomozygous58180426
4164938292164938293CT16GENIChomozygous58180428
4164938298164938299AG14GENIChomozygous58180430
4164939053164939054CT32GENIChomozygous58180434
4164939655164939656CT2GENICheterozygous58180436
4164939981164939982A-9GENIChomozygous58091590
4164940344164940345A-9GENIChomozygous58180438
4164940647164940648CA22GENICpossibly homozygous58180440
4164941015164941016GT25GENIChomozygous58180442
4164941243164941250TCCTAAG-------6GENICheterozygous58180444
4164941764164941765TC26GENICpossibly homozygous58180446
4164943134164943135CT22GENICheterozygous58180448
4164943202164943203CT33GENICpossibly homozygous58180450
4164943506164943507CA19GENICpossibly homozygous58180452
4164943920164943921AG19GENIChomozygous58180454
4164944181164944182TC27GENICpossibly homozygous57009616
4164944262164944263TG17GENIChomozygous57009617
4164944268164944269GA18GENIChomozygous58180456
4164944559164944560AG24GENICpossibly homozygous58180458
4164944765164944766CCTG16GENIChomozygous57009619
4164944796164944797GA13GENICpossibly homozygous58180460
4164946591164946592AG16GENIChomozygous57009623