chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188116211188116212CT50GENIChomozygous111146762
2188116254188116255GA48GENIChomozygous111146763
2188117050188117051CG31GENIChomozygous111146764
2188117570188117571CT41GENIChomozygous111146765
2188118098188118099AG32GENIChomozygous110168323
2188118153188118154AG16GENIChomozygous111146766
2188118298188118299GA31GENIChomozygous111146767
2188118514188118515GA37GENIChomozygous111146768
2188118594188118595GA58GENICheterozygous110168325
2188118636188118637TG52GENICheterozygous110168326
2188119322188119323AG29GENIChomozygous111146769
2188119406188119407CT27GENIChomozygous111146770
2188119560188119561AG20GENIChomozygous110168328
2188119726188119727TC21GENIChomozygous110168330
2188121102188121103CG26GENIChomozygous111146771
2188121186188121187AC27GENIChomozygous110168333
2188122240188122241TC17GENIChomozygous110804346
2188123316188123317AG47GENIChomozygous110804348
2188124385188124386GA29GENIChomozygous110804349
2188125449188125450AG27GENICpossibly homozygous110804350
2188125686188125687TC33GENICheterozygous110804351
2188125721188125722AG20GENIChomozygous110168336
2188125746188125747CT23GENIChomozygous110168338
2188128218188128219TC43GENIChomozygous110168342
2188128843188128844TA27GENIChomozygous110804353
2188129314188129315GA33GENIChomozygous111146772
2188130565188130566CT17GENICheterozygous111146773
2188130613188130614TC36GENICheterozygous111146774
2188130660188130661TC35GENICheterozygous111146775
2188135111188135112GA23GENIChomozygous110804355