chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5167675141167675142CG12GENIChomozygous114082552
5167678469167678470GA32GENIChomozygous114082554
5167681720167681721GA59GENIChomozygous114082555
5167682489167682490CT37GENICpossibly homozygous114082557
5167682789167682790AT33GENIChomozygous114082559
5167684610167684611TC60GENICheterozygous114082560
5167684841167684842GT52GENIChomozygous114082562
5167684881167684882AG36GENIChomozygous114082563
5167685112167685113GT20GENIChomozygous114082565
5167685511167685512TA80GENICheterozygous114082567
5167685915167685916GT41GENICheterozygous114082568
5167685919167685920GT40GENICpossibly homozygous114082570
5167686062167686063TC21GENICpossibly homozygous114082571
5167687196167687197TC54GENIChomozygous114082573
5167690165167690166GA34GENICheterozygous114082575
5167690169167690170AG33GENICheterozygous114082576
5167690333167690334GT52GENIChomozygous114082578
5167690565167690566AG39GENICpossibly homozygous114082579
5167690638167690639GA54GENIChomozygous114082581
5167691370167691371TA68GENICheterozygous114082582
5167691533167691534AG28GENIChomozygous114082584
5167691772167691773CT109GENICheterozygous114082585
5167691811167691812TC93GENICheterozygous114082587
5167691821167691822CT93GENICheterozygous114082588
5167692472167692473TC49GENIChomozygous114082590
5167692519167692520CT46GENIChomozygous114082591
5167692691167692692AG40GENIChomozygous114082593
5167692702167692703CT40GENIChomozygous114082594
5167692840167692841GA36GENIChomozygous114082596
5167693901167693902GT34GENIChomozygous114082597
5167694206167694207GT47GENIChomozygous114082599
5167694282167694283CT48GENIChomozygous114082600
5167694395167694396AT65GENICpossibly homozygous114082602
5167694456167694457GA36GENIChomozygous114082603
5167694841167694842TA21GENIChomozygous114082605
5167695495167695496TC40GENIChomozygous114082607
5167695797167695798AT54GENIChomozygous114082608