chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96489848864898489AC22GENIChomozygous117364557
96489980764899808GA28GENIChomozygous117364563
96490019564900196CT16GENIChomozygous117364567
96490041664900417GA24GENIChomozygous117547836
96490044764900448GT24GENIChomozygous117364569
96490202164902022TC26GENIChomozygous117364575
96490250964902510CT18GENIChomozygous117364577
96490259964902600TG18GENIChomozygous117364579
96490422764904228AG23GENIChomozygous117364581
96490464064904641GT25GENIChomozygous117364582
96490505964905060TC20GENIChomozygous117364584
96490637664906377GA11GENIChomozygous117364588
96490652764906528CT17GENIChomozygous117364590
96490702964907030CT8GENIChomozygous117364594
96490731264907313CT15GENIChomozygous117782909
96489993064899931TC36GENIChomozygous117782906
96490571264905713TC13GENIChomozygous117782907
96490613664906137GA17GENIChomozygous117782908
96490961464909615AT16GENIChomozygous117364596
96491015664910157TG20GENIChomozygous117782910
96491216564912166AG19GENIChomozygous117782911
96491290564912906AG22GENIChomozygous117364602
96491528664915287AG27GENIChomozygous117364606
96491559364915594CT21GENIChomozygous117364608
96491809764918098GA18GENIChomozygous117364612
96491925064919251GA15GENIChomozygous117364613
96492066764920668TC18GENIChomozygous117364615
96492156064921561AG18GENICpossibly homozygous117364621
96492227064922271CA17GENIChomozygous117782912
96492248964922490TC23GENIChomozygous117364627
96492298964922990AG15GENIChomozygous117364629