chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125213182125213183CA22GENIChomozygous956969434
1125213926125213927CT32GENIChomozygous956969435
1125214231125214232TC36GENIChomozygous956969436
1125214871125214872AG25GENIChomozygous956969437
1125214953125214954CT28GENIChomozygous956969438
1125215239125215240GA32GENIChomozygous956969439
1125217485125217486GA37GENIChomozygous956969440
1125218976125218977TC31GENIChomozygous956969441
1125221356125221357CT24GENIChomozygous956969442
1125224111125224112CT33GENICpossibly homozygous956969443
1125224413125224414AG35GENIChomozygous956969444
1125224784125224785TG16GENIChomozygous956969445
1125226171125226172TC16GENIChomozygous956969446
1125226820125226821GA39GENIChomozygous956969447
1125226862125226863GA33GENIChomozygous956969448
1125226934125226935GA34GENIChomozygous956969449
1125226967125226968CT35GENIChomozygous956969450
1125227266125227267CA17GENIChomozygous956969451
1125227267125227268CA15GENIChomozygous956969452
1125227268125227269CT15GENIChomozygous956969453
1125227524125227525CA22GENIChomozygous956969454
1125227655125227656GA19GENIChomozygous956969455
1125228013125228014TC14GENIChomozygous956969456
1125228026125228027AC15GENIChomozygous956969457
1125228141125228142GT14GENIChomozygous956969458
1125228215125228216CT13GENIChomozygous956969459
1125228275125228276CG17GENIChomozygous956969460
1125228284125228285TA17GENIChomozygous956969461
1125228363125228364TC17GENIChomozygous956969462
1125228434125228435TC18GENIChomozygous956969463
1125228819125228820CT26GENIChomozygous956969464
1125228884125228885AG24GENIChomozygous956969465
1125228896125228897TC26GENIChomozygous956969466