chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125213182125213183CA29GENIChomozygous783612414
1125213926125213927CT22GENIChomozygous783612415
1125214231125214232TC18GENIChomozygous783612416
1125214871125214872AG34GENIChomozygous783612417
1125214953125214954CT24GENIChomozygous783612418
1125215239125215240GA18GENIChomozygous783612419
1125215695125215696GA16GENICheterozygous783612420
1125215970125215971TC20GENICheterozygous783612421
1125215982125215983CT23GENICheterozygous783612422
1125217485125217486GA24GENIChomozygous783612423
1125218976125218977TC21GENIChomozygous783612424
1125221356125221357CT22GENIChomozygous783612425
1125224111125224112CT25GENIChomozygous783612426
1125224239125224240CA25GENIChomozygous783612427
1125224413125224414AG34GENIChomozygous783612428
1125226171125226172TC22GENIChomozygous783612429
1125226820125226821GA29GENIChomozygous783612430
1125226862125226863GA27GENIChomozygous783612431
1125226934125226935GA23GENIChomozygous783612432
1125226967125226968CT28GENIChomozygous783612433
1125227266125227267CA15GENIChomozygous783612434
1125227267125227268CA15GENIChomozygous783612435
1125227268125227269CT15GENIChomozygous783612436
1125227524125227525CA25GENIChomozygous783612437
1125227655125227656GA29GENIChomozygous783612438
1125228013125228014TC28GENIChomozygous783612439
1125228026125228027AC27GENICpossibly homozygous783612440
1125228141125228142GT23GENIChomozygous783612441
1125228215125228216CT23GENIChomozygous783612442
1125228275125228276CG27GENIChomozygous783612443
1125228284125228285TA28GENIChomozygous783612444
1125228363125228364TC25GENIChomozygous783612445
1125228434125228435TC24GENIChomozygous783612446
1125228819125228820CT21GENIChomozygous783612447
1125228884125228885AG11GENIChomozygous783612448
1125228896125228897TC15GENIChomozygous783612449