chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141293070141293077GTGAAGA12GENIChomozygous128529476
7141293368141293369TC26GENIChomozygous115939885
7141293544141293545AG17GENIChomozygous115939886
7141294733141294735CT19GENIChomozygous128529477
7141294751141294752TA20GENIChomozygous115939887
7141294849141294850CT20GENIChomozygous115939888
7141297108141297108A11GENICheterozygous128529478
7141297421141297422CA18GENIChomozygous115939889
7141297431141297432TG19GENIChomozygous115939890
7141299203141299204GA21GENIChomozygous115939891
7141303428141303429CT19GENIChomozygous115939892
7141304205141304206AG29GENIChomozygous115939893
7141308371141308371CAAA13GENIChomozygous128529480
7141308669141308669T5GENIChomozygous128529481