chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151821532918215330GA29GENIChomozygous142475057
151821798018217981CT18GENIChomozygous139680101
151821877818218779TG30GENIChomozygous139680102
151821979118219792AC6GENIChomozygous154933922
151822031518220316TC21GENIChomozygous139680103
151822089318220894GA25GENICpossibly homozygous139680104
151822140718221408A16GENIChomozygous139621081
151822269818222699GA24GENIChomozygous139680105
151822370318223704A21GENIChomozygous139621082
151822418018224181GA24GENIChomozygous139680106
151822436118224362TC20GENIChomozygous139680107
151822441818224419GA24GENIChomozygous139680108
151822535218225353CT27GENIChomozygous139680109
151822539118225392CT21GENIChomozygous139680110
151822545218225453TC20GENIChomozygous139680111
151822588818225889GA21GENIChomozygous139680112
151822623618226237GA28GENIChomozygous139680113
151822632018226321CT29GENIChomozygous139680114
151822645518226456CT22GENIChomozygous139680115
151822650218226503CA27GENIChomozygous139680116
151822663718226638TG30GENIChomozygous139680117
151822664018226641G27GENIChomozygous139621083
151822685518226856TC30GENIChomozygous139680118
151822696818226969GA23GENIChomozygous139680119
151822697018226971GA24GENIChomozygous139680120
151822724718227248CT30GENIChomozygous139680121
151822731718227318AG25GENIChomozygous139680122
151822741418227415GA33GENIChomozygous139680123
151822742918227430TC36GENIChomozygous139680124
151822755818227558GT15GENIChomozygous139621084
151822783218227833GA19GENIChomozygous139680125
151822862918228629TGATGAC20GENIChomozygous139621085