chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118894034118894035T21GENIChomozygous128637145
8118894043118894043T27GENIChomozygous128637146
8118894050118894050A28GENIChomozygous128637147
8118894072118894073TG33GENIChomozygous116674816
8118894226118894227TC41GENIChomozygous116674824
8118894088118894089TA39GENIChomozygous116674818
8118894091118894092CT40GENIChomozygous116674820
8118894225118894226TG41GENIChomozygous116674822
8118894239118894240TC40GENIChomozygous117062295
8118894357118894358TG64GENIChomozygous117062297
8118894412118894413GC65GENIChomozygous117062299
8118894413118894414GA65GENIChomozygous117062301
8118894541118894542AG50GENIChomozygous117062303
8118894970118894971AG60GENIChomozygous117062305
8118895278118895279GA68GENICpossibly homozygous117062307
8118895316118895317TC79GENICpossibly homozygous117062309
8118895362118895363AG75GENIChomozygous117062311
8118895441118895442GA77GENIChomozygous117062313
8118895556118895557AG64GENICpossibly homozygous117062315
8118895655118895656CT66GENIChomozygous117062317
8118895742118895743AG70GENIChomozygous117062319
8118895928118895929TC72GENIChomozygous117062321
8118896060118896061TC71GENIChomozygous117062323
8118896105118896106CT67GENIChomozygous117062325
8118896603118896604TC52GENIChomozygous117062327
8118896686118896687GC57GENIChomozygous117062329
8118896892118896893AC51GENIChomozygous117062331
8118896928118896929GA49GENIChomozygous117062333
8118897064118897065TG66GENIChomozygous117062335
8118899257118899258TC63GENIChomozygous116674848
8118910815118910816GA62GENIChomozygous117062337
8118894783118894783C65GENIChomozygous132125548
8118896811118896821ATGGGAGTGT66GENIChomozygous132125549
8118918641118918642AG66GENIChomozygous116675109
8118922780118922781AG73GENIChomozygous116675175
8118920847118920847AC12GENICheterozygous132322597