chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31127253811272539TG19GENIChomozygous111446476
31127285311272854AG22GENIChomozygous111446478
31127326411273265AG20GENIChomozygous111446484
31127380611273807AG18GENIChomozygous111446486
31127403411274035TC21GENIChomozygous111446488
31127446211274463TC18GENIChomozygous111446490
31127516711275168CA13GENICpossibly homozygous111446492
31127519211275193TC11GENIChomozygous111875600
31127525511275256CT17GENIChomozygous111446494
31127673411276735CA24GENIChomozygous111446496
31127709611277097CT24GENICpossibly homozygous111446498
31127710311277104AC23GENIChomozygous111446500