chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18054957680549577GT7GENIChomozygous109299070
18055103880551039TC10GENIChomozygous120481346
18055156880551569AG13GENIChomozygous120481347
18055700180557002TC6GENIChomozygous120839531
18055738680557387TC8GENIChomozygous109299078
18055790380557904CT15GENIChomozygous120868444
18055909180559092TC21GENIChomozygous120481348
18056091080560911TC12GENIChomozygous120481349
18056186980561870TC17GENIChomozygous120481350
18056206480562065TC11GENIChomozygous109299084
18056300680563007TC12GENIChomozygous109299086
18056477980564780AG6GENICheterozygous125482163
18056480180564802AT6GENIChomozygous120779216
18056604880566049AG21GENIChomozygous120481351
18056732080567321GC14GENIChomozygous125482164
18056733580567336GT5GENIChomozygous120839532
18056733780567338GT5GENIChomozygous120839533
18056733980567340GT4GENICheterozygous120839534
18056745980567460GA6GENIChomozygous120868450
18056857480568575CG11GENIChomozygous120481354
18056922080569221AG3GENICheterozygous125482165
18057075880570759AG22GENIChomozygous109299090
18057280880572809CT14GENIChomozygous120868451
18057312180573122GA22GENIChomozygous120868452
18057356180573562CT16GENIChomozygous120481356
18057479980574800AG11GENIChomozygous109299094
18057666680576667TC7GENICheterozygous121261410
18057942680579427TC14GENIChomozygous120481360
18058008380580084TC18GENIChomozygous120481361