chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
668804326880433TA64GENIChomozygous141801302
668804596880460AG64GENIChomozygous141801303
668809806880980CA54GENIChomozygous141774121
668812456881246TC59GENIChomozygous141801304
668817586881759AT62GENIChomozygous141801305
668818136881814AG68GENIChomozygous141801306
668825286882529GC49GENIChomozygous141801307
668837686883769GA57GENIChomozygous141801308
668845906884591AG52GENIChomozygous141801309
668848866884887AG59GENIChomozygous141801310
668884916888492CT58GENIChomozygous141801311
668898966889897AG59GENIChomozygous141801312
668905746890575AG16GENICpossibly homozygous141801313
668905766890577AG17GENIChomozygous141801314
668905786890579AG17GENIChomozygous141801315
668905806890581AG19GENIChomozygous141801316
668913846891385GA52GENIChomozygous141801317
668922006892201CT53GENIChomozygous141801318
668943466894350TTTG31GENIChomozygous141774122
668956606895661GA45GENIChomozygous141801319
668957096895710CT50GENIChomozygous141801320
668958036895804TC63GENIChomozygous141801321
668943316894332GT36GENIChomozygous154340988
668817586881759A62GENICheterozygous403165838
668943316894332G36GENICheterozygous403165839