chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105889674858896749CT31GENIChomozygous116607432
105889878258898783CT23GENIChomozygous116607434
105889943158899432AG37GENIChomozygous116607436
105889978558899786CT19GENIChomozygous116607438
105890028758900288GA16GENIChomozygous116607440
105890033058900331TA16GENIChomozygous116607442
105890061258900613CT23GENIChomozygous116607444
105890069058900691TG38GENIChomozygous116607446
105890187758901878CT14GENIChomozygous116607448
105890213058902131GA20GENIChomozygous116607450
105890796958907970CA31GENIChomozygous116607452
105891139258911393GA6GENIChomozygous116788076
105891257858912579TC18GENIChomozygous116607454
105891406258914063TC24GENIChomozygous116607456
105891623258916233CT16GENIChomozygous116607458
105891660858916609TC9GENIChomozygous116607460
105891685258916853TC24GENIChomozygous116607462
105891854958918550CT24GENIChomozygous116607464
105891886058918861CA20GENIChomozygous116607466
105891917158919172AG24GENIChomozygous116607468
105891954258919543TC19GENIChomozygous117219275
105892071058920711GT25GENIChomozygous116607470
105892159058921591TC20GENIChomozygous116607472
105892266358922664CT16GENIChomozygous116607474
105892402258924023TG23GENIChomozygous116607476