chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101355126413551265GC17GENIChomozygous126376050
101355127713551278GC13GENIChomozygous126376051
101355528113555282TC7GENIChomozygous116496234
101355568213555683TC11GENIChomozygous116496236
101355571113555712AG14GENIChomozygous116496238
101355722913557230CT14GENIChomozygous116735860
101355869913558700GA15GENIChomozygous116496242
101355870913558710AG14GENIChomozygous116496244
101355906613559067GA18GENIChomozygous116735862
101356032013560321AG18GENIChomozygous116496246
101356077613560777GA12GENIChomozygous116735864
101356143613561437AG7GENIChomozygous116735865
101356220813562209GA4GENICheterozygous126472931
101356312013563121TC23GENIChomozygous116735866
101356333713563338TG9GENIChomozygous116496252
101356348213563483CG19GENIChomozygous116735867
101356350213563503AG28GENIChomozygous116735868
101356413513564136AG11GENIChomozygous116496256
101356505313565054TC6GENIChomozygous116735869
101356576113565762CT11GENIChomozygous126376052
101356577513565776AG12GENIChomozygous116735870
101356645513566456AC20GENIChomozygous116496264
101356652913566530GA11GENICheterozygous116735871
101356694013566941CT10GENIChomozygous116735872
101356733813567339GT12GENIChomozygous116735873
101356772613567727TA15GENIChomozygous116496266
101356908013569081CT14GENIChomozygous116994656
101356953213569533AG14GENIChomozygous116496268
101356969313569694TC21GENIChomozygous116496270
101356982813569829CA11GENIChomozygous116859469
101357011013570111CT8GENIChomozygous116496272
101357018713570188CT9GENIChomozygous116735874
101357135713571358CT15GENIChomozygous116496274
101357192513571926GT28GENIChomozygous116735875
101357202913572030GT19GENIChomozygous116496276
101357339613573397TC16GENIChomozygous116496278
101357352713573528GA15GENIChomozygous116735876
101357389513573896CT10GENIChomozygous116735877
101357406113574062GA14GENIChomozygous116496280