chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2252458112252458113GT10GENICheterozygous110854663
2252458947252458948CT29GENICpossibly homozygous110854665
2252462564252462565CT38GENIChomozygous110854667
2252463142252463143TG37GENIChomozygous110854669
2252465009252465010CT42GENIChomozygous110854671
2252465896252465897GT44GENIChomozygous110389109
2252469003252469004CT40GENIChomozygous110854673
2252469087252469088CT35GENIChomozygous110854675
2252469658252469659AG41GENIChomozygous110854677
2252470116252470117CA30GENIChomozygous110854679
2252470184252470185AG54GENIChomozygous110854681
2252470225252470226GC51GENIChomozygous110854683
2252470597252470598TC58GENIChomozygous110389133
2252471010252471011GC46GENIChomozygous110389137
2252472189252472190AG33GENIChomozygous110389147
2252473476252473477AC61GENIChomozygous110389159
2252474003252474004GC45GENIChomozygous110854685
2252477192252477193TG14GENIChomozygous110854687
2252477884252477885TC44GENIChomozygous110389184
2252478701252478702CT39GENIChomozygous110854689
2252479037252479038AT30GENIChomozygous110389194
2252479952252479953TC51GENIChomozygous110854691
2252480019252480020TG48GENIChomozygous110389196
2252480570252480571GA46GENIChomozygous110854693
2252480881252480882TC32GENIChomozygous110854695
2252481214252481215GA24GENIChomozygous110854697
2252482108252482108AC11GENIChomozygous130880944
2252483005252483006GA48GENIChomozygous110389198
2252484322252484323TC41GENIChomozygous110389200
2252485214252485215CT41GENIChomozygous110389202
2252485270252485271CT36GENIChomozygous110389204
2252485300252485301AT39GENIChomozygous110854699
2252485669252485670CT44GENIChomozygous110854701
2252486350252486351A40GENIChomozygous127764772
2252486509252486509G12GENIChomozygous127764773
2252486528252486529GA14GENIChomozygous110854703
2252486735252486736TC28GENIChomozygous110389218
2252487231252487232GC33GENIChomozygous110389220
2252488169252488170CT48GENIChomozygous110389224
2252488149252488149A49GENIChomozygous132568720