chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
68015939380159394TC47GENIChomozygous115127584
68015982980159829CCCCGGTCGAACTGGAGAC46GENIChomozygous130982318
68015990180159902CT45GENIChomozygous115127585
68016046180160462TC40GENIChomozygous115127586
68016071980160720AC57GENIChomozygous115127587
68016080980160810CT43GENIChomozygous115127588
68016083680160841GGTTC39GENIChomozygous130982319
68016105380161054AG43GENIChomozygous115127590
68016108480161085TC46GENIChomozygous115127591
68016109380161094GC48GENIChomozygous115127592
68016171980161723TTTG34GENIChomozygous130982320
68016191080161911TC38GENIChomozygous115127593
68016196380161964AT35GENIChomozygous115127594
68016248180162481A28GENIChomozygous130982321
68016259180162592GT35GENIChomozygous115127595
68016336480163366AG36GENIChomozygous130982322
68016345680163457TC45GENIChomozygous115127598
68016358980163589T41GENICpossibly homozygous130982323
68016384780163848AG52GENIChomozygous115127599
68016397680163977GA46GENIChomozygous115127600
68016427880164279GA43GENIChomozygous115262912
68015988580159886CT48GENIChomozygous115262900
68015990080159901CT45GENIChomozygous115262902
68016085680160857GA41GENIChomozygous115262904
68016113980161140CT43GENIChomozygous115262906
68016155780161558GA39GENIChomozygous115262908
68016339480163395GA32GENIChomozygous115262910
68016248480162485TA27GENIChomozygous118574316
68016452280164523CA45GENIChomozygous115127601
68016472380164723TTGT45GENIChomozygous130982324
68016499380164994G48GENICpossibly homozygous130982325
68016502780165028AG55GENIChomozygous115127602
68016516080165161TA49GENIChomozygous115127603
68016525380165254GA47GENIChomozygous115127604
68016527680165277CT44GENIChomozygous115127605
68016553880165539AG27GENIChomozygous115127606
68016594580165946AG33GENIChomozygous115127607
68016633980166351CAGCCCCATTCT44GENIChomozygous128358170