chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1840831664083167AG35GENICpossibly homozygous110243339
1840831894083190GT35GENICpossibly homozygous110243341
1840844414084442GC38GENIChomozygous110243343
1840845574084558AC37GENICpossibly homozygous110243345
1840857494085750GA23GENIChomozygous110243347
1840860294086030AG50GENIChomozygous119478885
1840860344086035CT51GENICheterozygous119478886
1840860524086053GA54GENICheterozygous119478887
1840865604086561AG31GENIChomozygous110243349
1840873634087364CT30GENIChomozygous110243352
1840878794087880CT18GENIChomozygous110243354
1840881934088194TC25GENIChomozygous110243356
1840885324088533TC26GENIChomozygous110243358
1840888964088897GA23GENIChomozygous110243360
1840893774089378TC35GENIChomozygous110243362
1840897614089762CG31GENICheterozygous119478888
1840898454089846AC24GENIChomozygous110642088
1840898544089855AG27GENICpossibly homozygous110920098
1840921894092190AG55GENIChomozygous110243366
1840933984093399AG49GENIChomozygous110243368
1840934734093474TA45GENIChomozygous110243370
1840955754095576AG29GENIChomozygous110243372
1840960004096001TC36GENIChomozygous110243374
1840940334094034TC17GENIChomozygous110570997