chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832031278320313CT19GENIChomozygous798231932
47832062078320621AC31GENIChomozygous798231933
47832129278321293CT21GENIChomozygous798231934
47832214078322141CT26GENIChomozygous798231935
47832291378322914TA37GENIChomozygous798231936
47832524978325250CT15GENIChomozygous798231937
47832595578325956AG28GENIChomozygous798231938
47832624978326250GA38GENIChomozygous798231939
47832635778326358GA40GENIChomozygous798231940
47832674778326748CT37GENIChomozygous798231941
47832682978326830TC41GENIChomozygous798231942
47832703778327038TC31GENIChomozygous798231943
47832710578327106CA26GENIChomozygous798231944