chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132828942132828943GA40GENIChomozygous116905484
8132829194132829195CT47GENIChomozygous116905486
8132831177132831178GA52GENIChomozygous116905488
8132832819132832820TC47GENIChomozygous116730002
8132834594132834595AG23GENIChomozygous116905490
8132835630132835631TC49GENIChomozygous116730009
8132835847132835848CG52GENIChomozygous116905492
8132835992132835993AG65GENIChomozygous116905494
8132836100132836101AG39GENIChomozygous116905496
8132836252132836253GT36GENIChomozygous116730010
8132836459132836460GA45GENIChomozygous116905498
8132836539132836540GA50GENIChomozygous116905500
8132836550132836551CA56GENIChomozygous116905502
8132836608132836609AG56GENIChomozygous116905504
8132836902132836903TG41GENIChomozygous116905506
8132837174132837175AC42GENIChomozygous116905508
8132837196132837197TC43GENIChomozygous116905510
8132838025132838026GT55GENIChomozygous116905512
8132838253132838254GA50GENIChomozygous116905514
8132838389132838390GA42GENIChomozygous116905516
8132838490132838491TC32GENIChomozygous116905518
8132838681132838682AT38GENIChomozygous116905520
8132839257132839258CT59GENIChomozygous116905522
8132839373132839374TG50GENIChomozygous116730011
8132839601132839602TC30GENIChomozygous116905524
8132840641132840642TC33GENICpossibly homozygous116905526