chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188590875188590879CTCT22GENIChomozygous127717445
2188590913188590923TTTTTTAAAG15GENIChomozygous127717446
2188590925188590926TG15GENIChomozygous127826380
2188590927188590950ATTTATTTATTTATTTATTATAA15GENIChomozygous127717447
2188590959188590960AT12GENIChomozygous127826381
2188591847188591848TC35GENIChomozygous110169450
2188592089188592090AG52GENIChomozygous110169452
2188592099188592100CG50GENIChomozygous110169454
2188592633188592636GAG49GENICpossibly homozygous127717451
2188590955188590955AATACA13GENIChomozygous127717448
2188591545188591545A33GENICpossibly homozygous127717449
2188591562188591562AAATA35GENIChomozygous127717450
2188593513188593514G43GENIChomozygous127717452
2188593575188593576TC55GENIChomozygous110169456
2188593753188593753C53GENIChomozygous127717453
2188594113188594114G47GENICpossibly homozygous127717454
2188595205188595206CT44GENIChomozygous110169458
2188595629188595630CT48GENIChomozygous110169460