chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108631568486315685CT22GENIChomozygous950578647
108632007386320074GT7GENIChomozygous950578648
108632117686321177AG12GENIChomozygous950578649
108632129686321297GA5GENIChomozygous950578650
108632166286321663GA10GENIChomozygous950578651
108632169186321692GA10GENIChomozygous950578652
108632223486322235CT9GENIChomozygous950578653
108632232886322329CT6GENIChomozygous950578654
108632233386322334AG8GENIChomozygous950578655
108632967086329671CT9GENIChomozygous950578656
108633074986330750CT12GENIChomozygous950578657
108633105086331051AG7GENIChomozygous950578658
108633150886331509AG11GENIChomozygous950578659
108633257886332579GT7GENIChomozygous950578660
108633384986333850CT5GENIChomozygous950578661
108633405486334055TC12GENIChomozygous950578662
108633464086334641AG8GENIChomozygous950578663
108633483586334836TC5GENIChomozygous950578664
108633575886335759GA6GENIChomozygous950578665