chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29158109491581095AG16GENIChomozygous136215577
29158120091581201CT21GENIChomozygous136215578
29158134091581341CT10GENIChomozygous136215579
29158169191581692TA29GENIChomozygous141401039
29158246491582465GA25GENIChomozygous136215580
29158255491582555CA20GENIChomozygous136215581
29158308791583089AT28GENIChomozygous135927780
29158317991583180AG23GENIChomozygous136215582
29158367991583680GA24GENIChomozygous141401040
29158410091584101TC23GENIChomozygous136215583
29158411391584114TC24GENIChomozygous136215584
29158445191584452TC12GENIChomozygous136215585
29158445991584460GC12GENIChomozygous136215586
29158446291584463TC12GENIChomozygous136215587
29158446991584470TC12GENIChomozygous136215588
29158450491584505GA6GENIChomozygous136215589
29158451191584512TC4GENIChomozygous141401041
29158477391584774TC14GENIChomozygous136215590
29158486591584866C14GENIChomozygous403012183
29158486591584866CT14GENICheterozygous403012184
29158486091584861T14GENIChomozygous403012181
29158486091584861TC14GENICheterozygous403012182
29158490691584907TC14GENICheterozygous153959480
29158490691584907T14GENIChomozygous403012185
29158491891584919GA14GENIChomozygous136215591
29158517891585179CT22GENIChomozygous141401042
29158547691585477CG15GENIChomozygous141401043
29158549591585496TC14GENIChomozygous141401044