chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1174301826174301827AG6GENICheterozygous62026293
1174301848174301849AC8GENICheterozygous62026296
1174301898174301899GA11GENICheterozygous62026297
1174301913174301914GC13GENICheterozygous62026298
1174301915174301916AG13GENICheterozygous62026299
1174301941174301942AG17GENICheterozygous62026300
1174301957174301958TC17GENICheterozygous62026301
1174301963174301964CA17GENICheterozygous62026302
1174301968174301969CT17GENICheterozygous62026303
1174301969174301970AG17GENICheterozygous62026304
1174301973174301974TC17GENICheterozygous62026305
1174301996174301997GA23GENICheterozygous62026306
1174302006174302007GA24GENICheterozygous62026307
1174302108174302109AG59GENICheterozygous62026308
1174302109174302110TC59GENICheterozygous62026309
1174302142174302143AG64GENICheterozygous62026310
1174302189174302190GA59GENICheterozygous62026311
1174302207174302208TG55GENICheterozygous62026312
1174302229174302230T-45GENICheterozygous62026313
1174302287174302288CG88GENICheterozygous62026314
1174302343174302344AG91GENICheterozygous62026315
1174302371174302372CT74GENICheterozygous62026316
1174302394174302395AC71GENICheterozygous62026317
1174302407174302408TC66GENICheterozygous62026318