chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125128240351282404CT50GENIChomozygous115355106
125128256451282565CA36GENIChomozygous118274983
125128274451282745TC72GENIChomozygous115355108
125128778751287788GA65GENIChomozygous115355110
125128864751288648CT47GENIChomozygous115355112
125129053251290533GA50GENICpossibly homozygous115355114
125129078151290782TC43GENIChomozygous115355116
125129115651291157GC40GENIChomozygous115355118
125129182251291823TC54GENICpossibly homozygous115355120
125129363451293635CT62GENIChomozygous115430682
125129580451295805CT9GENICheterozygous118274984
125129637551296376CA23GENIChomozygous118274985
125129637851296379AC23GENIChomozygous118274986
125129690951296910TC25GENICheterozygous118274987
125129825251298253AG55GENIChomozygous115355126
125129830051298301TA66GENIChomozygous115355128
125129830851298309AT64GENIChomozygous115355130
125129935451299355CA45GENIChomozygous115355132
125129996051299961AG39GENIChomozygous115355134
125130310451303105TC43GENICheterozygous118274988
125130334951303350GA50GENIChomozygous115355136
125130523051305231TC50GENIChomozygous115355138
125130548851305489AG42GENIChomozygous115355140
125130779051307791GT48GENIChomozygous115355142
125130897151308972GT36GENICpossibly homozygous115355145
125131015451310155GA26GENICheterozygous115633593
125131127751311278GA48GENIChomozygous115355147
125131343351313434GA63GENIChomozygous115355149
125131424551314246TC44GENIChomozygous115355151
125131725351317254GA24GENIChomozygous115355153
125131841051318411TC52GENIChomozygous115430686
125131855451318555CA16GENIChomozygous115404422
125133133851331339GA44GENIChomozygous115355155
125133997751339978GT22GENIChomozygous115355157
125134005751340058CG26GENIChomozygous115355159
125134034451340345AG48GENICpossibly homozygous115355161
125134081751340818AG17GENIChomozygous118274989
125134100951341010AG31GENIChomozygous115355163
125134141451341415GA25GENIChomozygous115355165
125134158051341581TC28GENIChomozygous115355167