chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG27GENIChomozygous975813574
5172491197172491198CT21GENIChomozygous975813575
5172491314172491315CT14GENIChomozygous975813576
5172491996172491997TC17GENIChomozygous975813577
5172492247172492248TC11GENIChomozygous975813578
5172492253172492254CT11GENIChomozygous975813579
5172493271172493272CT20GENIChomozygous975813580
5172493291172493292GA12GENIChomozygous975813581
5172493570172493571GC31GENIChomozygous975813582
5172494808172494809TC26GENIChomozygous975813583
5172494883172494884CT21GENIChomozygous975813584
5172496684172496685CT20GENIChomozygous975813585
5172496946172496947TC17GENIChomozygous975813586
5172499650172499651GA16GENIChomozygous975813587
5172499683172499684AG10GENIChomozygous975813588
5172499955172499956CT11GENIChomozygous975813589
5172505834172505835GA7GENIChomozygous975813590
5172514486172514487GA18GENIChomozygous975813591
5172517554172517555CT14GENIChomozygous975813592
5172522126172522127AG25GENIChomozygous975813593
5172525073172525074TC30GENIChomozygous975813594
5172541982172541983AT9INTERGENIChomozygous975813595