chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141759686717596867T52GENICheterozygous129129608
141759739917597400AG54GENIChomozygous113362682
141759770817597709AG53GENIChomozygous113662447
141759858117598582A29GENICpossibly homozygous129129610
141760129217601297ATTAA30GENIChomozygous132181725
141760316017603161AG53GENIChomozygous113662449
141760319817603199CT55GENIChomozygous113662451
141760734417607345GA45GENIChomozygous113662453
141760837317608373GAGGACATTTACA52GENIChomozygous129129618
141760886017608860AC55GENIChomozygous129129619
141761200017612001CT43GENIChomozygous113662455
141761258917612589CT54GENIChomozygous131726955
141761298117612982GA42GENIChomozygous113662457
141761343717613438GC54GENIChomozygous113662459
141761361317613614GA57GENIChomozygous113362764
141761548117615482CT51GENIChomozygous113662461
141761598617615987TC49GENIChomozygous113362766
141761606817616069G30GENICpossibly homozygous130139216