chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129976815129976816GA21GENIChomozygous115888858
7129977964129977965CA13GENIChomozygous118259838
7129982969129982970CT39GENIChomozygous116345674
7129984891129984892GA34GENIChomozygous115888883
7129988791129988792GA50GENIChomozygous116345676
7129994726129994727TC71GENIChomozygous115888985
7129994904129994905AG20GENICpossibly homozygous115888987
7129995120129995121CT27GENIChomozygous116345686
7129997896129997897TC46GENIChomozygous115888993
7129999568129999569CT48GENIChomozygous116345688
7130015273130015274AG25GENIChomozygous116345692
7130021503130021504TC53GENIChomozygous115889081
7130022583130022584GA34GENIChomozygous116345694
7130022984130022985TC48GENIChomozygous115889085
7130026780130026781AG34GENIChomozygous115889099
7130027384130027385CT32GENIChomozygous116345696
7130036423130036424CT33GENIChomozygous116345698
7130036628130036629CT47GENIChomozygous116345700