chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91562121315621214CT21GENIChomozygous117680504
91562151315621514TC26GENIChomozygous117680506
91562158015621581AG22GENIChomozygous117673062
91562172115621722CG24GENIChomozygous117680508
91562187115621872AC14GENIChomozygous117673066
91562189215621893CA16GENIChomozygous117673068
91562193715621938TC17GENIChomozygous117680510
91562220115622202AG21GENIChomozygous117673072
91562234315622344AG9GENIChomozygous117673074
91562242615622427AG14GENIChomozygous117673076
91562248915622490GT2GENIChomozygous117792136
91562249315622494AC2GENIChomozygous117792138
91562318115623182TC7GENIChomozygous117673080
91562395715623958CT16GENIChomozygous117792140
91562417015624171GA27GENIChomozygous117680512
91562422715624228CT24GENICpossibly homozygous117680514
91562426515624266GA16GENIChomozygous117680516
91562489415624895AG26GENIChomozygous117680518
91562494315624944GA24GENIChomozygous117680520
91562499415624995CT21GENIChomozygous117268034
91562515115625152AG20GENIChomozygous117680522
91562533615625337AG23GENIChomozygous117680524
91562563515625636CT30GENIChomozygous117680526
91562577615625777CT42GENIChomozygous120362498
91562587915625880TC29GENIChomozygous117680528
91562658115626582CT31GENIChomozygous117673102
91562666215626663AC26GENIChomozygous117268035
91562667215626673TA23GENIChomozygous117268036
91562668815626689AG23GENIChomozygous117673104
91562698615626987CG27GENIChomozygous117680530
91562721915627220CT21GENIChomozygous117680532
91562743115627432CT12GENIChomozygous117680534
91562785815627859CT30GENIChomozygous117680536
91562799015627991CT23GENIChomozygous117268037
91562801215628013AG18GENIChomozygous117268038
91562842715628428CT29GENIChomozygous117680538
91562849215628493TC21GENIChomozygous117680540
91562895115628952AG24GENIChomozygous117268040