chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2148813106148813107TC4GENIChomozygous974942098
2148813668148813669AG32GENIChomozygous974942099
2148814120148814121CA30GENIChomozygous974942100
2148819000148819001GA15GENIChomozygous974942101
2148820469148820470GA13GENIChomozygous974942102
2148820511148820512GA13GENIChomozygous974942103
2148824855148824856CT15GENIChomozygous974942104
2148824893148824894AG21GENIChomozygous974942105
2148825110148825111GC22GENICpossibly homozygous974942106
2148827232148827233TG22GENIChomozygous974942107
2148827357148827358AG27GENICpossibly homozygous974942108
2148827942148827943CT36GENIChomozygous974942109
2148828900148828901AT23GENIChomozygous974942110
2148829010148829011GA28GENIChomozygous974942111
2148830940148830941AG21GENIChomozygous974942112
2148833615148833616TC2GENIChomozygous974942113
2148833771148833772TC17GENIChomozygous974942114
2148835738148835739GA18GENIChomozygous974942115
2148837557148837558AC13GENIChomozygous974942116
2148838252148838253GT4GENIChomozygous974942117
2148840582148840583CA34GENIChomozygous974942118
2148842201148842202AG19GENIChomozygous974942119
2148847716148847717GA24GENIChomozygous974942120
2148848271148848272GA38GENIChomozygous974942121
2148848596148848597TC33GENIChomozygous974942122
2148848891148848892CT18GENIChomozygous974942123
2148849918148849919CT26GENIChomozygous974942124
2148851545148851546CT22GENICpossibly homozygous974942125
2148852097148852098CG17GENICpossibly homozygous974942126
2148852161148852162AG26GENICpossibly homozygous974942127
2148852365148852366CT33GENIChomozygous974942128
2148853817148853818CA23GENIChomozygous974942129
2148854259148854260CT28GENIChomozygous974942130
2148854560148854561AG31GENIChomozygous974942131
2148854999148855000CT25GENIChomozygous974942132
2148855469148855470CT30GENIChomozygous974942133
2148855596148855597TC18GENIChomozygous974942134
2148856963148856964TG23GENIChomozygous974942135
2148857621148857622TC23GENIChomozygous974942136
2148858378148858379AG35GENIChomozygous974942137