chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166501824065018241CT14GENIChomozygous142566625
166501826565018266T16GENIChomozygous142515941
166501870065018701GC48GENIChomozygous142566626
166502000365020004GA54GENIChomozygous142566627
166502202365022024TG49GENIChomozygous142566631
166502185065021851AG50GENIChomozygous142566630
166502094065020941GC48GENIChomozygous142566628
166502095665020957CT47GENIChomozygous142566629
166502202965022030G47GENIChomozygous142515942
166502209065022091CT42GENIChomozygous142566632
166502499165024992GT36GENIChomozygous142566634
166502670365026704TC32GENIChomozygous142566635
166502706865027069CT40GENIChomozygous142566636
166503048265030483CA56GENIChomozygous142566637
166503407265034073TA48GENIChomozygous142566638
166503010665030107C38GENIChomozygous403401085
166502202965022030GT47GENICheterozygous154959483
166503010665030107CG38GENICheterozygous154959486