chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18259636982596370AG37GENIChomozygous109561146
18259653082596531TC30GENIChomozygous108878304
18259750182597502CT16GENICheterozygous108878305
18259752782597528CT17GENICheterozygous108878306
18259754582597546TC16GENICheterozygous109561147
18259775782597758TC17GENIChomozygous108878307
18259807882598079CG34GENIChomozygous109561148
18259940182599402TC36GENIChomozygous108878310
18259956982599570AC11GENIChomozygous108140572
18259971982599720GC15GENIChomozygous108140574
18259989382599894AG42GENIChomozygous108878311
18259993482599935GA43GENIChomozygous109561149
18260021382600214CT13GENIChomozygous109561150
18260159482601595AG26GENIChomozygous108878315
18260199382601994AT10GENICpossibly homozygous108140575
18260234682602347GA36GENICpossibly homozygous109561151
18260265982602660TC3GENIChomozygous109561152
18260275882602759GA22GENIChomozygous109561153
18260426882604269AC39GENIChomozygous109302620
18260510582605106GA35GENIChomozygous108878318
18260523982605240TC35GENIChomozygous108878319
18260563082605631AG44GENIChomozygous109561154
18260612682606127CT9GENICheterozygous109302622
18260617582606176TC15GENIChomozygous108878322
18260626682606267CT25GENIChomozygous108878323
18260658782606588CG3GENIChomozygous108878324
18260672182606722TA11GENIChomozygous108878325
18260677182606772GA21GENIChomozygous108878326
18260794782607948CT35GENIChomozygous108878328
18260852482608525TC49GENIChomozygous108878329
18260897782608978CT27GENIChomozygous108878330
18260965782609658TG16GENIChomozygous108140576
18260977782609778AC7GENIChomozygous108140577
18260977882609779TC7GENIChomozygous108140578
18260986082609861TG25GENIChomozygous108140579
18260996482609965TC10GENIChomozygous108140580