chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173632750173632751TC41GENIChomozygous108389458
1173649414173649415TG65GENICheterozygous109168883
1173649757173649758GA78GENICheterozygous109168885
1173650240173650241TC78GENICheterozygous108756550
1173650253173650254AC89GENICheterozygous108756554
1173650287173650288CT84GENICheterozygous108389488
1173651219173651220TC141GENICheterozygous108756556
1173651220173651221GA140GENICheterozygous108756558
1173651228173651229CT135GENICheterozygous108756560
1173651236173651237TC132GENICheterozygous108389494
1173652783173652784AG79GENICheterozygous108389506
1173652818173652819GA106GENICheterozygous108756570
1173652885173652886AT106GENICheterozygous108389514
1173652925173652926CA83GENICheterozygous108389516
1173659087173659088CT21GENIChomozygous108389524
1173665142173665143CA24GENIChomozygous108389544
1173650734173650735AC52GENIChomozygous108961255
1173667395173667396CT194GENICheterozygous109168887
1173674759173674760GA66GENIChomozygous108961259
1173680574173680575CT35GENIChomozygous108389604
1173681476173681477TA51GENIChomozygous108961260