chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205672065205672066CT43GENICpossibly homozygous510467090
1205672463205672464TTTTTTCTTTTC36GENIChomozygous685154111
1205672468205672469CCT42GENICheterozygous685154112
1205672498205672499TC53GENIChomozygous510467091
1205680581205680582TC39GENIChomozygous507201576
1205680853205680854G-27GENIChomozygous685154113
1205681421205681422CCAA18GENIChomozygous685154114
1205682221205682222CCTT23GENIChomozygous685154115
1205682304205682305CA44GENICpossibly homozygous507201577
1205682571205682572CT64GENIChomozygous507201578