chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96489848864898489AC8GENIChomozygous117364557
96489980764899808GA25GENIChomozygous117364563
96490019564900196CT23GENIChomozygous117364567
96490041664900417GA27GENICpossibly homozygous117547836
96490044764900448GT27GENICpossibly homozygous117364569
96490202164902022TC26GENIChomozygous117364575
96490250964902510CT21GENIChomozygous117364577
96490259964902600TG30GENIChomozygous117364579
96490422764904228AG28GENIChomozygous117364581
96490464064904641GT36GENIChomozygous117364582
96490505964905060TC25GENIChomozygous117364584
96490637664906377GA29GENIChomozygous117364588
96490652764906528CT30GENIChomozygous117364590
96490702964907030CT30GENIChomozygous117364594
96490731264907313CT22GENIChomozygous117782909
96489993064899931TC39GENIChomozygous117782906
96490571264905713TC33GENIChomozygous117782907
96490613664906137GA38GENIChomozygous117782908
96490961464909615AT35GENIChomozygous117364596
96491015664910157TG27GENIChomozygous117782910
96491216564912166AG36GENIChomozygous117782911
96491290564912906AG36GENIChomozygous117364602
96491528664915287AG31GENIChomozygous117364606
96491559364915594CT26GENIChomozygous117364608
96491809764918098GA29GENIChomozygous117364612
96491925064919251GA25GENIChomozygous117364613
96492066764920668TC15GENIChomozygous117364615
96492227064922271CA33GENIChomozygous117782912
96492248964922490TC35GENIChomozygous117364627
96492298964922990AG34GENIChomozygous117364629