chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184055562740555628CT24GENIChomozygous110329405
184055835940558360AG21GENIChomozygous110329407
184055925640559257TG13GENICpossibly homozygous110329409
184055977840559779CT29GENIChomozygous110329411
184055984740559848TC17GENIChomozygous110329413
184056006040560061GA23GENIChomozygous110329415
184056029840560299TA23GENIChomozygous110329417
184056204240562043TC12GENIChomozygous110329419
184056222740562228TA14GENIChomozygous110329421
184056251040562511AT24GENIChomozygous110329423
184056426240564263GA26GENIChomozygous110329425
184056468340564684AG28GENIChomozygous110329427
184056646940566470CT25GENIChomozygous110329429
184056648740566488GC21GENIChomozygous110329431
184056718840567189GA19GENIChomozygous110329433
184056768240567683CT19GENIChomozygous110329435
184056812640568127CA9GENIChomozygous110329437
184057042640570427GA45GENIChomozygous110329439
184057042940570430GA44GENIChomozygous110329441
184057045140570452CT44GENIChomozygous110329443
184057045440570455CA42GENIChomozygous110329445
184057049540570496CT40GENICpossibly homozygous110329447
184057124040571241TC21GENIChomozygous110329449
184057155940571560CA6GENIChomozygous110684245
184057221140572212AG17GENIChomozygous110329453
184057253540572536AG16GENIChomozygous110329455