chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160123496160123497TC44GENIChomozygous114073873
5160126878160126879TC20GENIChomozygous114073890
5160127108160127109CT29GENIChomozygous114073891
5160127865160127866TA47GENIChomozygous114073892
5160130094160130095CA27GENIChomozygous114160513
5160131405160131406GA37GENIChomozygous114073895
5160132176160132177CT21GENIChomozygous114160516
5160133516160133517AG39GENIChomozygous114073897
5160135065160135066TA29GENIChomozygous114073898
5160135140160135141CT10GENIChomozygous114073899
5160136568160136569AG22GENIChomozygous114073906
5160137298160137299GA40GENIChomozygous114160517
5160140920160140921AT24GENIChomozygous114073911
5160141398160141399GA32GENIChomozygous114160519
5160143389160143390GT38GENIChomozygous114160520
5160144527160144528CT38GENIChomozygous114160521
5160144560160144561CT39GENIChomozygous114160522
5160145654160145655TC36GENIChomozygous114073917
5160149058160149059GA10GENIChomozygous119106539
5160155927160155928CG28GENIChomozygous114160527
5160157062160157063GT31GENIChomozygous114160530
5160157605160157606CT18GENIChomozygous114160531
5160157765160157766GC46GENIChomozygous114160532
5160158284160158285GA41GENIChomozygous114160533