chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29158109491581095AG69GENIChomozygous136215577
29158120091581201CT57GENIChomozygous136215578
29158134091581341CT17GENIChomozygous136215579
29158169191581692TA46GENIChomozygous141401039
29158246491582465GA55GENIChomozygous136215580
29158255491582555CA48GENIChomozygous136215581
29158308791583089AT62GENIChomozygous135927780
29158367991583680GA44GENIChomozygous141401040
29158411391584114TC34GENIChomozygous136215584
29158317991583180AG56GENIChomozygous136215582
29158410091584101TC36GENIChomozygous136215583
29158445191584452TC20GENIChomozygous136215585
29158445991584460GC20GENIChomozygous136215586
29158446291584463TC20GENIChomozygous136215587
29158446991584470TC19GENIChomozygous136215588
29158450491584505GA7GENIChomozygous136215589
29158451191584512TC7GENIChomozygous141401041
29158477391584774TC19GENIChomozygous136215590
29158486591584866C43GENIChomozygous403012183
29158486591584866CT43GENICheterozygous403012184
29158486091584861T43GENIChomozygous403012181
29158486091584861TC43GENICheterozygous403012182
29158490691584907TC43GENICheterozygous153959480
29158490691584907T43GENIChomozygous403012185
29158491891584919GA45GENIChomozygous136215591
29158517891585179CT53GENIChomozygous141401042
29158547691585477CG44GENIChomozygous141401043
29158549591585496TC49GENIChomozygous141401044