chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2148875730148875731CT28GENICpossibly homozygous110050329
2148876901148876902TG11GENIChomozygous110050335
2148877800148877801CG18GENIChomozygous110050336
2148877883148877884TC16GENIChomozygous110050337
2148878525148878526TC24GENIChomozygous110050338
2148879948148879949CG21GENIChomozygous110050339
2148880009148880010CT16GENIChomozygous110050340
2148883146148883147GA22GENIChomozygous110050341
2148883729148883730GA5GENIChomozygous110050342
2148884321148884322GA5GENIChomozygous110050343
2148886666148886667TG20GENIChomozygous110050344
2148886830148886831GA24GENIChomozygous110050345
2148887242148887243TC31GENIChomozygous110050346
2148888053148888054AG23GENIChomozygous110050347
2148888184148888185CT8GENIChomozygous110050348
2148888370148888371AG18GENIChomozygous110050349
2148888678148888679GA13GENIChomozygous110050350
2148888694148888695CT11GENIChomozygous110050351
2148889016148889017CT15GENIChomozygous110050352
2148889206148889207GA26GENIChomozygous110050353
2148889494148889495GT18GENIChomozygous110050354
2148889501148889502TC18GENIChomozygous110050355
2148889532148889533GC25GENIChomozygous110050356
2148890085148890086AG17GENIChomozygous110050357
2148890319148890320TA24GENIChomozygous110050358
2148890557148890558GT17GENIChomozygous110050359
2148890813148890814TC17GENIChomozygous110050360