chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2148875730148875731CT11GENIChomozygous110050329
2148876312148876313GA6GENIChomozygous110050331
2148876657148876658AG6GENIChomozygous110050332
2148876659148876660GA7GENIChomozygous110050333
2148876708148876709CT3GENICheterozygous110050334
2148876901148876902TG13GENIChomozygous110050335
2148877800148877801CG20GENIChomozygous110050336
2148877883148877884TC10GENIChomozygous110050337
2148878525148878526TC14GENIChomozygous110050338
2148879948148879949CG26GENIChomozygous110050339
2148880009148880010CT19GENIChomozygous110050340
2148883146148883147GA22GENIChomozygous110050341
2148883729148883730GA17GENIChomozygous110050342
2148884321148884322GA18GENIChomozygous110050343
2148886666148886667TG25GENIChomozygous110050344
2148886830148886831GA19GENIChomozygous110050345
2148887242148887243TC14GENICheterozygous110050346
2148888053148888054AG16GENIChomozygous110050347
2148888184148888185CT5GENICheterozygous110050348
2148888370148888371AG22GENIChomozygous110050349
2148888678148888679GA16GENICheterozygous110050350
2148888694148888695CT12GENIChomozygous110050351
2148889016148889017CT28GENIChomozygous110050352
2148889206148889207GA24GENIChomozygous110050353
2148889494148889495GT16GENIChomozygous110050354
2148889532148889533GC22GENIChomozygous110050356
2148890085148890086AG6GENIChomozygous110050357
2148890319148890320TA20GENIChomozygous110050358
2148890813148890814TC16GENIChomozygous110050360
2148891018148891019CA14GENIChomozygous110050361