chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151821877818218779TG26GENIChomozygous139680102
151821922918219230GA15GENIChomozygous143621021
151821979118219792AC10GENIChomozygous154933922
151822031518220316TC15GENIChomozygous139680103
151822285618222857CT17GENIChomozygous143621022
151822436118224362TC14GENIChomozygous139680107
151822479318224794CT20GENIChomozygous143621023
151822535218225353CT10GENIChomozygous139680109
151822539118225392CT10GENIChomozygous139680110
151822545218225453TC14GENIChomozygous139680111
151822588818225889GA17GENIChomozygous139680112
151822610918226110CT21GENIChomozygous143621024
151822623618226237GA19GENIChomozygous139680113
151822632018226321CT18GENIChomozygous139680114
151822645518226456CT12GENIChomozygous139680115
151822650218226503CA11GENIChomozygous139680116
151822663718226638TG17GENIChomozygous139680117
151822685518226856TC13GENIChomozygous139680118
151822696818226969GA19GENIChomozygous139680119
151822697018226971GA19GENIChomozygous139680120
151822724718227248CT18GENIChomozygous139680121
151822731718227318AG20GENIChomozygous139680122
151822741418227415GA18GENIChomozygous139680123
151822742918227430TC20GENIChomozygous139680124
151822862918228629TGATGAC18GENIChomozygous139621085
151822370318223704A19GENICpossibly homozygous139621082
151822664018226641G17GENIChomozygous139621083
151822755818227558GT16GENIChomozygous139621084
151822263118222631ATGATGATG7GENIChomozygous143603596
151822676918226770G24GENIChomozygous143603597