chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221116244221116245TC31GENIChomozygous108543592
1221117378221117379TC30GENIChomozygous108543594
1221117612221117613AG29GENIChomozygous108543596
1221117935221117936AG64GENIChomozygous108543598
1221118700221118701GC44GENIChomozygous108543600
1221120091221120092TC32GENIChomozygous108543602
1221121319221121320AG38GENIChomozygous108543604
1221122233221122234AG39GENIChomozygous108543606
1221124956221124957AG43GENIChomozygous108543622
1221126210221126211AG18GENIChomozygous108543624
1221126369221126370CT45GENIChomozygous108543626
1221127906221127907CT52GENICpossibly homozygous108543628
1221129084221129085TA41GENIChomozygous108543630