chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197965503197965504TC16GENIChomozygous125306851
1197965799197965800AT17GENIChomozygous108496494
1197966641197966642GA13GENIChomozygous108496496
1197969926197969927GT19GENIChomozygous108496498
1197970480197970481CT20GENIChomozygous108496500
1197971610197971611GA27GENIChomozygous108496504
1197972050197972051CT15GENIChomozygous108496506
1197972480197972481AG4GENIChomozygous108496508
1197972481197972482AG4GENIChomozygous108496510
1197972483197972484TG5GENIChomozygous108496512
1197975539197975540TC14GENIChomozygous108496518
1197976696197976697GA18GENIChomozygous108496520
1197977239197977240TC14GENIChomozygous108496524
1197977316197977317CT11GENIChomozygous108496526
1197977996197977997TC19GENIChomozygous108496530
1197979075197979076GA15GENIChomozygous108496532
1197979259197979260AT19GENIChomozygous108496534
1197979936197979937AC17GENIChomozygous108496536
1197981780197981781GA11GENICheterozygous108496538
1197981851197981852CT55GENICheterozygous108496540
1197981858197981859GT24GENICheterozygous108496542
1197981871197981872CT24GENICheterozygous108496544
1197981875197981876AG25GENICheterozygous108496546
1197981891197981892CG32GENICheterozygous108496548
1197982553197982554AG20GENICheterozygous108496556
1197982588197982589CG19GENICheterozygous108496562
1197982620197982621AG13GENICheterozygous108496564
1197982624197982625TC13GENICheterozygous108496566
1197982713197982714TC65GENICheterozygous108496568