chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75363102053631021TG18GENIChomozygous115685774
75363296753632968AG21GENIChomozygous115685776
75363369553633696TC30GENIChomozygous115685777
75363422253634223AG39GENIChomozygous115685778
75363584553635846TA19GENIChomozygous115685779
75363589353635894TC25GENIChomozygous115685780
75363590253635903AG27GENIChomozygous115685781
75363591453635915CT30GENIChomozygous115685782
75363605053636051CT37GENIChomozygous115685783
75363631753636318TG32GENIChomozygous115685784
75363670053636701AG24GENIChomozygous115685785
75363680353636804TA29GENIChomozygous115685786
75363722653637227TG23GENIChomozygous115685787
75363789353637894TA28GENIChomozygous115685789
75363885753638858AG23GENIChomozygous115685790
75363887353638874GA22GENIChomozygous115685791
75363899653638997GA30GENIChomozygous115685792
75363929453639295GT33GENIChomozygous115685793
75363933953639340AG33GENIChomozygous115685794
75363952053639521GA27GENIChomozygous115685795
75363991553639916TC24GENIChomozygous115685796
75364039753640398TA34GENIChomozygous115685797
75364059653640597TC41GENIChomozygous115685798
75364072753640728GA46GENIChomozygous115685799
75364099253640993CA22GENIChomozygous115685800
75364247853642479CT27GENIChomozygous115685801
75364286153642862GT16GENIChomozygous115685802
75364483253644833GC27GENIChomozygous116290118
75364584453645845AG33GENIChomozygous115685803
75364669253646693AT28GENIChomozygous115685804
75364791253647913GT39GENIChomozygous116290119
75364828453648285AG28GENIChomozygous115685806
75364864553648646AC37GENIChomozygous116290120
75364868153648682CT30GENIChomozygous116290121