chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111422494111422495GT17GENIChomozygous990458709
3111423384111423385CT16GENIChomozygous990458710
3111424281111424282TC14GENIChomozygous990458711
3111425983111425984GC17GENIChomozygous990458712
3111427053111427054GC19GENIChomozygous990458713
3111428965111428966AG5GENIChomozygous990458714
3111429442111429443TC4GENIChomozygous990458715
3111429609111429610AC11GENIChomozygous990458716
3111430237111430238GA21GENIChomozygous990458717
3111431398111431399GA16GENIChomozygous990458718
3111432156111432157GA25GENIChomozygous990458719
3111432680111432681GA19GENIChomozygous990458720
3111434551111434552CA11GENIChomozygous990458721
3111436304111436305AG25GENIChomozygous990458722
3111437233111437234TG15GENIChomozygous990458723
3111439046111439047GC7GENIChomozygous990458724
3111439159111439160CT11GENIChomozygous990458725
3111439677111439678CT11GENIChomozygous990458726
3111440006111440007AG5GENIChomozygous990458727
3111441752111441753CT19GENIChomozygous990458728
3111444789111444790CT12GENIChomozygous990458729
3111445266111445267AG21GENIChomozygous990458730
3111445739111445740GA16GENIChomozygous990458731
3111446036111446037TC23GENIChomozygous990458732
3111446091111446092TG17GENIChomozygous990458733
3111446383111446384TC12GENIChomozygous990458734
3111446875111446876AT16GENIChomozygous990458735
3111451135111451136TC22GENIChomozygous990458736