chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166501824065018241CT9GENIChomozygous142566625
166501826565018266T15GENIChomozygous142515941
166501870065018701GC48GENIChomozygous142566626
166502000365020004GA34GENIChomozygous142566627
166502094065020941GC53GENIChomozygous142566628
166502095665020957CT52GENIChomozygous142566629
166502185065021851AG43GENIChomozygous142566630
166502202365022024TG41GENIChomozygous142566631
166502202965022030G41GENIChomozygous142515942
166502209065022091CT37GENIChomozygous142566632
166502499165024992GT44GENIChomozygous142566634
166502670365026704TC38GENIChomozygous142566635
166502706865027069CT43GENIChomozygous142566636
166503048265030483CA57GENIChomozygous142566637
166503407265034073TA54GENIChomozygous142566638
166503010665030107C34GENIChomozygous403401085
166502202965022030GT41GENICheterozygous154959483
166503010665030107CG34GENICheterozygous154959486