chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10111309537111309538AT30GENICheterozygous502977220
10111309785111309786GA4GENICheterozygous502977221
10111309838111309839TG11GENICheterozygous505935843
10111311177111311178TC11GENICheterozygous505935844
10111311279111311280CT11GENICheterozygous505935845
10111311394111311395TC35GENICheterozygous505935846
10111311447111311448TC27GENICheterozygous505935847
10111311501111311502TC16GENICheterozygous505935848
10111311517111311518AC16GENICheterozygous505935849
10111311526111311527CT18GENICheterozygous505935850
10111311567111311568GA17GENICheterozygous505935851
10111311614111311615AG16GENICheterozygous505935852
10111318895111318896CG20GENICheterozygous502977222
10111318966111318967T-19GENICheterozygous684433183
10111318994111318995AC22GENICheterozygous502977223
10111319632111319633TC18GENICheterozygous505935853
10111320871111320872TC27GENICheterozygous505935854
10111320895111320896GA22GENICheterozygous505935855
10111321330111321331GC66GENICheterozygous505935856
10111321728111321729CA96GENICheterozygous505935857
10111321754111321755CA136GENICheterozygous505935858