chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168600588168600589TC5GENIChomozygous112944500
4168602207168602208TA21GENIChomozygous112944502
4168604305168604306AG14GENIChomozygous112944504
4168604990168604991GA8GENIChomozygous112944506
4168605125168605126AG18GENIChomozygous112944508
4168605498168605499CG11GENIChomozygous112944510
4168607837168607838TC17GENIChomozygous112944512
4168607845168607846CT18GENIChomozygous112944514
4168608776168608777TC7GENIChomozygous112944516
4168608941168608942CG6GENICheterozygous126029006
4168609454168609455GA8GENIChomozygous112944518
4168611323168611324GA28GENIChomozygous112944520
4168613711168613712AG22GENIChomozygous112944522
4168615382168615383TC12GENIChomozygous112944524
4168617933168617934TC18GENIChomozygous112944526
4168618273168618274AT22GENIChomozygous112944528
4168618381168618382AG20GENIChomozygous112944530
4168618452168618453GA12GENIChomozygous112944532
4168618649168618650GA25GENIChomozygous112944534
4168618807168618808CA5GENIChomozygous112944536
4168619916168619917CT6GENICheterozygous126029007
4168619917168619918TC6GENICheterozygous126029008
4168619945168619946TC32GENIChomozygous112944538
4168621601168621602AG4GENIChomozygous112944542
4168621994168621995TA5GENIChomozygous112944544
4168622293168622294TC14GENIChomozygous112944558
4168622475168622476AT28GENIChomozygous112944560
4168622780168622781AT25GENIChomozygous112944562
4168623262168623263GA24GENIChomozygous112944564
4168624539168624540CT12GENIChomozygous112944566
4168624564168624565TC19GENIChomozygous112944568
4168624891168624892CT21GENIChomozygous112944570