chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121738327817383279A-16GENIChomozygous50718514
121738395917383963CACT----21GENICpossibly homozygous50718516
121738408517384086GA21GENIChomozygous50718518
121738408617384087GA21GENIChomozygous50718520
121738591417385915TC37GENIChomozygous50718521
121738652717386528A-12GENIChomozygous50600456
121738738517387386TG22GENIChomozygous50718523
121738741517387416TC21GENIChomozygous50718525
121738688817386889AAAGTTCCTG21GENIChomozygous50733595
121738688717386888CCTGTGG20GENIChomozygous50733593