chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151821532918215330GA28GENIChomozygous142475057
151821798018217981CT24GENIChomozygous139680101
151821877818218779TG26GENIChomozygous139680102
151821979118219792AC10GENIChomozygous154933922
151822031518220316TC18GENIChomozygous139680103
151822089318220894GA26GENIChomozygous139680104
151822140718221408A22GENIChomozygous139621081
151822269818222699GA22GENIChomozygous139680105
151822370318223704A24GENICpossibly homozygous139621082
151822418018224181GA22GENIChomozygous139680106
151822436118224362TC30GENIChomozygous139680107
151822441818224419GA22GENIChomozygous139680108
151822535218225353CT26GENIChomozygous139680109
151822539118225392CT25GENIChomozygous139680110
151822545218225453TC28GENIChomozygous139680111
151822588818225889GA22GENIChomozygous139680112
151822623618226237GA16GENIChomozygous139680113
151822632018226321CT20GENIChomozygous139680114
151822645518226456CT25GENIChomozygous139680115
151822650218226503CA29GENIChomozygous139680116
151822663718226638TG21GENIChomozygous139680117
151822664018226641G21GENIChomozygous139621083
151822685518226856TC26GENIChomozygous139680118
151822696818226969GA25GENIChomozygous139680119
151822697018226971GA25GENIChomozygous139680120
151822724718227248CT26GENIChomozygous139680121
151822731718227318AG19GENIChomozygous139680122
151822741418227415GA20GENIChomozygous139680123
151822742918227430TC17GENIChomozygous139680124
151822755818227558GT19GENIChomozygous139621084
151822783218227833GA24GENIChomozygous139680125
151822862918228629TGATGAC16GENIChomozygous139621085