chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
66011457860114579AG18GENIChomozygous114824108
66011527960115280CT42GENIChomozygous114824110
66011586860115869AG57GENIChomozygous114824112
66011593360115934AG62GENIChomozygous114824114
66011613360116134CT33GENIChomozygous114824116
66011634460116345GC34GENICpossibly homozygous114824118
66011670860116709GA68GENIChomozygous114824120
66011688860116889GA60GENIChomozygous114824122
66011693560116936CA47GENIChomozygous114824124
66011695860116959AG46GENIChomozygous114824126
66011728760117288TC58GENIChomozygous114824128
66011751160117512GA51GENIChomozygous114824130
66011760360117604TG59GENIChomozygous114824132
66011778460117785TG25GENIChomozygous114824134
66011820760118208TC34GENIChomozygous114824136
66011845460118455GA59GENIChomozygous114824137
66011900760119008GC49GENIChomozygous114824139
66011943660119437TC53GENIChomozygous114824141
66011980160119802TC39GENIChomozygous114824143
66012018860120189TC43GENIChomozygous114824145
66012069060120691GT35GENIChomozygous114824147
66012117360121174CT69GENIChomozygous114824149
66012238960122390GT39GENIChomozygous114824151
66012257560122576AC9GENIChomozygous114824153
66012257960122580CT9GENIChomozygous114824155
66012267060122671CT16GENIChomozygous114824157
66012281260122813TC42GENIChomozygous114824159
66012285560122856GA15GENIChomozygous114824161
66012292960122930CT32GENIChomozygous114824163
66012315160123152AG32GENIChomozygous114824165
66012319860123199AG38GENIChomozygous114824167
66012361660123617CT50GENIChomozygous114824169
66012404060124041GA50GENIChomozygous114824171