chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104740024447400245TC9GENIChomozygous116773595
104740118147401182TC5GENIChomozygous116773597
104740266847402669TG7GENIChomozygous116773599
104740287447402875TC5GENIChomozygous116773601
104740494347404944AG6GENIChomozygous116773603
104740513147405132CT2GENIChomozygous116773605
104740681447406815TC13GENIChomozygous116773607
104740880647408807AG10GENIChomozygous116773609
104740908947409090AG12GENIChomozygous116773611
104740913647409137GA10GENIChomozygous116773613
104740961547409616AG6GENIChomozygous116773615
104740967547409676GC12GENIChomozygous116773617
104741423947414240AG5GENIChomozygous116773619
104741581047415811AG7GENIChomozygous116773621
104741618547416186GA6GENIChomozygous116773623
104741637547416376AG12GENIChomozygous116773625
104741710347417104TC18GENIChomozygous116773627
104741808147418082AG21GENIChomozygous116773629
104741827347418274CT11GENIChomozygous116773631
104741864747418648GA12GENIChomozygous116773633
104741907147419072GA6GENIChomozygous116773635
104741928247419283AG12GENIChomozygous116773637
104741935347419354CT8GENIChomozygous116773639
104742024147420242CT7GENIChomozygous116773641
104742156147421562CT7GENIChomozygous116773643