chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3102576037102576038GGT6GENICheterozygous58617922
3102585055102585056GA9GENIChomozygous57579565
3102585057102585058TTTA9GENIChomozygous57579567
3102585059102585063GCCC----9GENIChomozygous57579569
3102585066102585067GGAA7GENIChomozygous57579571
3102585072102585073GT6GENIChomozygous57579573
3102585073102585074CT6GENIChomozygous57579575
3102585185102585193ACATCCCA--------9GENIChomozygous57579589
3102585196102585197CG6GENIChomozygous57938865
3102585209102585210AT10GENIChomozygous57579591
3102585231102585232CT13GENIChomozygous57938868
3102585232102585233AC12GENIChomozygous57938871
3102595407102595408TTCTTTTC8GENIChomozygous57579593
3102624718102624719CT29GENIChomozygous58168227
3102624726102624727GA28GENIChomozygous57938980
3102633712102633714AC--10GENICheterozygous58670810
3102637216102637217GA23GENIChomozygous58168229