chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151821532918215330GA50GENIChomozygous142475057
151821798018217981CT39GENIChomozygous139680101
151821877818218779TG49GENIChomozygous139680102
151821979118219792AC14GENIChomozygous154933922
151822031518220316TC46GENIChomozygous139680103
151822089318220894GA49GENIChomozygous139680104
151822269818222699GA54GENIChomozygous139680105
151822418018224181GA50GENIChomozygous139680106
151822436118224362TC60GENIChomozygous139680107
151822441818224419GA58GENIChomozygous139680108
151822535218225353CT51GENIChomozygous139680109
151822539118225392CT54GENIChomozygous139680110
151822545218225453TC46GENIChomozygous139680111
151822588818225889GA35GENIChomozygous139680112
151822623618226237GA45GENIChomozygous139680113
151822632018226321CT43GENIChomozygous139680114
151822645518226456CT44GENIChomozygous139680115
151822650218226503CA43GENICpossibly homozygous139680116
151822663718226638TG49GENIChomozygous139680117
151822685518226856TC43GENIChomozygous139680118
151822696818226969GA36GENIChomozygous139680119
151822697018226971GA35GENIChomozygous139680120
151822724718227248CT47GENIChomozygous139680121
151822731718227318AG43GENIChomozygous139680122
151822741418227415GA49GENIChomozygous139680123
151822742918227430TC48GENIChomozygous139680124
151822783218227833GA61GENIChomozygous139680125
151822755818227558GT50GENIChomozygous139621084
151822140718221408A46GENIChomozygous139621081
151822370318223704A55GENIChomozygous139621082
151822664018226641G49GENIChomozygous139621083
151822862918228629TGATGAC39GENIChomozygous139621085
151822265718222675GATGATGATGATGATGAC49GENIChomozygous142457682