chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267607530267607531GA46GENICpossibly homozygous108640323
1267608826267608827GA63GENIChomozygous108640325
1267608829267608830TC69GENIChomozygous108640326
1267609268267609269GA36GENIChomozygous108785143
1267609504267609505CA52GENIChomozygous108785144
1267609548267609549GA51GENIChomozygous108785145
1267609856267609857GA59GENIChomozygous108785146
1267610232267610233AG44GENIChomozygous108785147
1267610402267610403GA60GENIChomozygous108785148
1267610507267610508CT62GENIChomozygous108785149
1267610670267610671CT55GENIChomozygous108785150
1267610679267610680TC54GENIChomozygous108785151
1267610757267610758AG54GENIChomozygous108785152
1267610775267610776CT45GENIChomozygous108785153
1267610875267610876GT9GENIChomozygous108785154
1267610985267610986CT46GENIChomozygous108785155
1267611057267611058CT57GENIChomozygous108785156
1267611752267611753GA57GENIChomozygous108785157
1267612073267612074GA56GENICpossibly homozygous108785158
1267615318267615319CT57GENIChomozygous108785161
1267612324267612325AG69GENIChomozygous108785159
1267614387267614388CT49GENIChomozygous108785160
1267614470267614471GA69GENIChomozygous108640332
1267615641267615642AG52GENIChomozygous108640334
1267616016267616017TC55GENICpossibly homozygous108785162
1267616383267616384TC58GENIChomozygous108785163
1267616701267616702CT55GENICheterozygous108785164