chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1237328483732849TG3GENIChomozygous67541276
1237390623739063C17GENICheterozygous67424709
1237390623739063CA3GENIChomozygous67541278
1237367113736712CT14GENIChomozygous66913355
1237374943737495AG8GENIChomozygous66913357
1237393793739380AT26GENIChomozygous66913361
1237419463741947G6GENICheterozygous67541280
1237419803741981A7GENICheterozygous67541286
1237419803741981A7GENICheterozygous67541282
1237419803741980A7GENICheterozygous67541284
1237419803741980A7GENICheterozygous67541289
1237432633743264GA17GENIChomozygous66913365
1237433053743306GA22GENIChomozygous66913367
1237473613747362TC10GENIChomozygous66913373
1237482093748210CG25GENIChomozygous66599608
1237482993748300CT19GENIChomozygous66913375
1237484233748424CA16GENIChomozygous66599609
1237491843749185AC25GENIChomozygous66913377
1237509203750921AG11GENIChomozygous66913379
1237528233752824AG20GENIChomozygous66913381
1237539233753924AG17GENIChomozygous66913383
1237539873753988AG13GENIChomozygous66913385
1237541803754181GA11GENIChomozygous66913387
1237542883754289GT16GENIChomozygous66913389
1237547023754702A12GENICheterozygous67541291
1237622193762220AG17GENIChomozygous66913405
1237547843754785CT10GENIChomozygous66913391
1237557633755764TG3GENIChomozygous67541293
1237567203756721AG17GENIChomozygous66913399
1237574763757477CA24GENIChomozygous66913401
1237579073757908AG18GENIChomozygous66913403
1237601103760111GC3GENIChomozygous67541295
1237613023761303AG21GENIChomozygous66599616
1237642553764256TC22GENIChomozygous66599623
1237689693768970GT19GENIChomozygous66913435
1237690383769039GA14GENIChomozygous66599625
1237691143769115TG10GENIChomozygous66913437
1237691343769135GC13GENICheterozygous66599626
1237691433769144CT12GENIChomozygous66913440
1237691843769185CG20GENIChomozygous66599627
1237702253770226TC8GENIChomozygous66913443