chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1237338673733868AG12GENIChomozygous66599605
1237367113736712CT16GENIChomozygous66913355
1237374943737495AG11GENIChomozygous66913357
1237390623739063C9GENIChomozygous67424709
1237393793739380AT17GENIChomozygous66913361
1237432633743264GA9GENIChomozygous66913365
1237433053743306GA17GENIChomozygous66913367
1237473613747362TC29GENICheterozygous66913373
1237482093748210CG27GENIChomozygous66599608
1237482993748300CT22GENIChomozygous66913375
1237484233748424CA13GENIChomozygous66599609
1237491843749185AC13GENIChomozygous66913377
1237509203750921AG21GENIChomozygous66913379
1237528233752824AG17GENIChomozygous66913381
1237539233753924AG17GENIChomozygous66913383
1237539873753988AG15GENIChomozygous66913385
1237541803754181GA29GENIChomozygous66913387
1237542883754289GT16GENIChomozygous66913389
1237547843754785CT13GENIChomozygous66913391
1237567203756721AG21GENIChomozygous66913399
1237574763757477CA20GENIChomozygous66913401
1237579073757908AG21GENIChomozygous66913403
1237613023761303AG15GENIChomozygous66599616
1237622193762220AG18GENIChomozygous66913405
1237642553764256TC28GENIChomozygous66599623
1237678983767899GA6GENIChomozygous66599624
1237689693768970GT26GENIChomozygous66913435
1237690383769039GA20GENIChomozygous66599625
1237691143769115TG12GENIChomozygous66913437
1237691343769135GC12GENIChomozygous66599626
1237691433769144CT13GENIChomozygous66913440
1237691843769185CG12GENIChomozygous66599627
1237702253770226TC7GENIChomozygous66913443
1237547023754702A15GENICheterozygous67609236