chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142912116142912117TG28GENIChomozygous114034012
5142912484142912485GA28GENIChomozygous114034013
5142915062142915063TC18GENIChomozygous114034014
5142915512142915513TC11GENIChomozygous114034015
5142918315142918316AG2GENIChomozygous132090059
5142917964142917965AG3GENICheterozygous128301444
5142921092142921093GT6GENICheterozygous128301454
5142921096142921097GT7GENICheterozygous129923908
5142921188142921189CA9GENICheterozygous131404136
5142924506142924507GA26GENIChomozygous114034018
5142924565142924566CT26GENIChomozygous114034019
5142924698142924699CT20GENIChomozygous114034020
5142926562142926563TC14GENIChomozygous114034021
5142926983142926984GA17GENIChomozygous114034022
5142927181142927182CT22GENIChomozygous114034023
5142927977142927978TC25GENIChomozygous114034024
5142928367142928368GA20GENIChomozygous114034025
5142931700142931701GA18GENIChomozygous114034026
5142931913142931914AG26GENIChomozygous114034027
5142932697142932698TG4GENIChomozygous132090065