chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116108913116108914TC32GENIChomozygous53305582
8116109030116109031AG26GENIChomozygous52827433
8116109321116109322AG27GENICpossibly homozygous52827434
8116109529116109530CCCCTT16GENIChomozygous52827436
8116109599116109600GA23GENIChomozygous53305583
8116109837116109838TC27GENIChomozygous52827437
8116110635116110636CT37GENIChomozygous53305584
8116111137116111138CT38GENIChomozygous53305585
8116112150116112151AG16GENIChomozygous52827440
8116112345116112346CCA15GENIChomozygous52827441
8116112564116112565CT33GENIChomozygous52827443
8116113093116113094GA21GENIChomozygous53305586
8116113783116113784GGA13GENIChomozygous52827445
8116114055116114056TC23GENIChomozygous52827446
8116114778116114779CA33GENIChomozygous52827447
8116115028116115029CT31GENIChomozygous52827448
8116115724116115727TTT---2GENIChomozygous52827449
8116115800116115801CG24GENIChomozygous52827450
8116115860116115861GA25GENIChomozygous52827451
8116117009116117010C-34GENIChomozygous52827452
8116117013116117014AT36GENIChomozygous52827453
8116119030116119031CG39GENIChomozygous52827455
8116119931116119932TTAAA7GENIChomozygous52827457
8116119934116119935GGATATGACCT3GENIChomozygous52827458
8116120149116120151AA--15GENIChomozygous53305587
8116120225116120227TT--23GENIChomozygous53305588
8116121000116121001GA22GENICpossibly homozygous53305589