chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125213182125213183CA17GENIChomozygous885100323
1125213926125213927CT13GENIChomozygous885100324
1125214231125214232TC22GENIChomozygous885100325
1125214871125214872AG24GENIChomozygous885100326
1125214953125214954CT19GENIChomozygous885100327
1125215239125215240GA12GENIChomozygous885100328
1125217485125217486GA21GENICpossibly homozygous885100329
1125218976125218977TC27GENIChomozygous885100330
1125221356125221357CT30GENIChomozygous885100331
1125224111125224112CT22GENIChomozygous885100332
1125224239125224240CA29GENIChomozygous885100333
1125224413125224414AG15GENIChomozygous885100334
1125226171125226172TC7GENIChomozygous885100335
1125226820125226821GA32GENIChomozygous885100336
1125226862125226863GA17GENIChomozygous885100337
1125226934125226935GA15GENIChomozygous885100338
1125226967125226968CT17GENIChomozygous885100339
1125227524125227525CA12GENIChomozygous885100340
1125227655125227656GA25GENIChomozygous885100341
1125228013125228014TC12GENICheterozygous885100342
1125228026125228027AC7GENICheterozygous885100343
1125228141125228142GT19GENIChomozygous885100344
1125228215125228216CT17GENIChomozygous885100345
1125228275125228276CG11GENIChomozygous885100346
1125228284125228285TA11GENIChomozygous885100347
1125228363125228364TC11GENIChomozygous885100348
1125228434125228435TC20GENIChomozygous885100349
1125228819125228820CT17GENIChomozygous885100350