chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142119923142119924AG33GENIChomozygous108262697
1142124615142124616AT38GENIChomozygous108262699
1142125016142125017TC31GENIChomozygous108262701
1142125842142125843CG48GENICheterozygous108262703
1142126035142126036CT40GENICpossibly homozygous108262705
1142127242142127243TC32GENIChomozygous108262707
1142127521142127522AG42GENIChomozygous108262709
1142127896142127897AG43GENIChomozygous108262711
1142130850142130851CG33GENIChomozygous108262715
1142134040142134041CT53GENIChomozygous108262717
1142135092142135093CG38GENICpossibly homozygous108262719