chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171053957610539577AG14GENIChomozygous968146760
171054242110542422AG33GENIChomozygous968146761
171054274510542746TC21GENIChomozygous968146762
171054305810543059TC30GENIChomozygous968146763
171054340610543407CT41GENIChomozygous968146764
171054360310543604AG32GENIChomozygous968146765
171054376810543769CG17GENIChomozygous968146766
171054455010544551TC31GENIChomozygous968146767
171054506710545068AG16GENIChomozygous968146768
171054586110545862CT23GENIChomozygous968146769
171054682510546826AG37GENIChomozygous968146770
171054696010546961TC26GENICpossibly homozygous968146771
171054748810547489GA37GENIChomozygous968146772