chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151821877818218779TG19GENIChomozygous139680102
151821922918219230GA20GENIChomozygous143621021
151821979118219792AC5GENIChomozygous154933922
151822031518220316TC23GENIChomozygous139680103
151822285618222857CT16GENIChomozygous143621022
151822436118224362TC17GENIChomozygous139680107
151822479318224794CT14GENIChomozygous143621023
151822535218225353CT22GENIChomozygous139680109
151822539118225392CT17GENIChomozygous139680110
151822545218225453TC22GENIChomozygous139680111
151822588818225889GA20GENIChomozygous139680112
151822610918226110CT22GENIChomozygous143621024
151822623618226237GA16GENIChomozygous139680113
151822632018226321CT18GENIChomozygous139680114
151822645518226456CT21GENIChomozygous139680115
151822650218226503CA23GENICpossibly homozygous139680116
151822663718226638TG24GENIChomozygous139680117
151822685518226856TC18GENIChomozygous139680118
151822696818226969GA13GENIChomozygous139680119
151822697018226971GA13GENIChomozygous139680120
151822724718227248CT19GENIChomozygous139680121
151822731718227318AG21GENIChomozygous139680122
151822741418227415GA28GENIChomozygous139680123
151822742918227430TC23GENIChomozygous139680124
151822664018226641G24GENIChomozygous139621083
151822263118222631ATGATGATG6GENIChomozygous143603596
151822676918226770G21GENIChomozygous143603597
151822370318223704A14GENIChomozygous139621082
151822755818227558GT10GENIChomozygous139621084
151822862918228629TGATGAC13GENIChomozygous139621085