chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103671632136716322GT16GENIChomozygous116561632
103671663236716633TC9GENIChomozygous116561634
103671799636717997AG19GENIChomozygous116561638
103671900836719009TC18GENIChomozygous116759703
103671910136719102AG22GENIChomozygous116561640
103671989236719893GA16GENIChomozygous116561642
103672187836721879AG17GENIChomozygous116561646
103672193236721933AG27GENIChomozygous116561648
103672310436723105TC29GENIChomozygous116561650
103672325336723254TC14GENIChomozygous116561652
103672347936723480AC5GENICheterozygous126441358
103672515336725154AG26GENIChomozygous116561654
103672679336726794AG18GENIChomozygous116759705
103672778336727784GC19GENIChomozygous116561656
103672888436728885TA21GENIChomozygous116561658
103672940836729409CT4GENICheterozygous126441359
103672965136729652AG15GENIChomozygous116759707
103673006936730070AT13GENICheterozygous116561660
103673007036730071GC13GENIChomozygous116561662
103673278236732783CG24GENIChomozygous116561668
103673343236733433CT11GENIChomozygous116561670
103673344036733441TG7GENIChomozygous116561672