chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1799749239974924AC15GENIChomozygous111572705
1799760409976041GA36GENIChomozygous111230339
1799763659976366TC36GENIChomozygous111332235
1799768349976835AG35GENIChomozygous110953498
1799769159976916TC35GENIChomozygous110953502
1799772339977234AG33GENIChomozygous111167228
1799774589977459AG22GENIChomozygous111230342
1799774629977463AG26GENIChomozygous110953504
1799775769977577AG27GENIChomozygous110953506
1799779409977941CT31GENIChomozygous110953508
1799785829978583AG24GENIChomozygous110953510
1799788909978891GT35GENIChomozygous110953512
1799791739979174CT35GENIChomozygous111230344
1799794469979447CT35GENIChomozygous111230346
1799797439979744CT31GENIChomozygous110953514
1799798199979820CT42GENIChomozygous110953516
1799808339980834CA26GENICpossibly homozygous111167230
1799811519981152AC27GENIChomozygous110953520
1799816449981645AT34GENIChomozygous110953522
1799818329981833CT30GENIChomozygous111230348
1799819189981919TC28GENIChomozygous110953524
1799819469981947CT14GENIChomozygous110953526
1799783649978365TC31GENIChomozygous111495637
1799825799982580TC29GENIChomozygous110953530
1799823579982358TC18GENICpossibly homozygous119263895
1799823599982360AG18GENICpossibly homozygous119263896
1799823829982383AG27GENIChomozygous119263897
1799784269978427CT9GENICheterozygous119370892
1799810609981061TC12GENICheterozygous119370893
1799820289982029TC8GENIChomozygous119370894
1799809589980959TC9GENIChomozygous111315058