chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75363102053631021TG9GENIChomozygous115685774
75363296753632968AG13GENIChomozygous115685776
75363369553633696TC27GENIChomozygous115685777
75363422253634223AG30GENIChomozygous115685778
75363584553635846TA14GENIChomozygous115685779
75363589353635894TC15GENIChomozygous115685780
75363590253635903AG17GENIChomozygous115685781
75363591453635915CT17GENIChomozygous115685782
75363605053636051CT17GENIChomozygous115685783
75363631753636318TG20GENIChomozygous115685784
75363670053636701AG10GENIChomozygous115685785
75363680353636804TA16GENIChomozygous115685786
75363722653637227TG13GENIChomozygous115685787
75363789353637894TA22GENIChomozygous115685789
75363885753638858AG17GENIChomozygous115685790
75363887353638874GA20GENIChomozygous115685791
75363899653638997GA24GENIChomozygous115685792
75363929453639295GT14GENIChomozygous115685793
75363933953639340AG13GENIChomozygous115685794
75363952053639521GA24GENIChomozygous115685795
75363991553639916TC20GENIChomozygous115685796
75364039753640398TA23GENIChomozygous115685797
75364059653640597TC14GENIChomozygous115685798
75364072753640728GA27GENIChomozygous115685799
75364099253640993CA26GENIChomozygous115685800
75364286153642862GT22GENIChomozygous115685802
75364584453645845AG35GENIChomozygous115685803
75364669253646693AT17GENIChomozygous115685804
75364828453648285AG7GENIChomozygous115685806
75364483253644833GC21GENIChomozygous116290118
75364791253647913GT29GENIChomozygous116290119
75364864553648646AC17GENIChomozygous116290120
75364868153648682CT21GENIChomozygous116290121