chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102900388102900389CG13GENIChomozygous109115303
1102901884102901886TG9GENIChomozygous130818462
1102902990102902991AG12GENIChomozygous109115305
1102903115102903115T13GENIChomozygous130818463
1102904457102904458GA7GENIChomozygous109115307
1102905859102905860CT14GENIChomozygous109115309
1102906236102906237TC17GENIChomozygous109115311
1102906280102906281CA18GENIChomozygous109115313
1102906321102906322TC21GENIChomozygous109115315
1102906857102906858TG21GENIChomozygous109115317
1102906861102906862AC22GENIChomozygous109115319
1102906877102906878T16GENIChomozygous130818464
1102906990102906991AG13GENIChomozygous109115321
1102907239102907240CT16GENIChomozygous109115323
1102907754102907755GA19GENIChomozygous109115325
1102908286102908287AT22GENIChomozygous109115327
1102908597102908598AG18GENIChomozygous109115329
1102909621102909622TC18GENICpossibly homozygous109115335
1102909313102909314GC14GENICheterozygous108735406
1102909001102909004AGG9GENIChomozygous130818465
1102909589102909589TA17GENICheterozygous130818466