chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186068914460689145CCA11GENIChomozygous46948921
186068914560689146CG11GENIChomozygous46948922
186069022160690223AC--2GENICheterozygous46948923
186069061060690611CT19GENICpossibly homozygous46479984
186069175160691752CT25GENICpossibly homozygous46948925
186069227660692277TG17GENICheterozygous46479986
186069445560694456GGC8GENIChomozygous46665798
186069467160694672CA15GENICheterozygous46479990
186069509860695099AG16GENIChomozygous46479992
186069688460696885AC23GENICpossibly homozygous46948926
186069711060697111GT22GENIChomozygous46479996
186069726060697261TG12GENIChomozygous46479997
186069749460697495AG19GENIChomozygous46479998
186069767460697675CT12GENIChomozygous46479999
186069768060697681CG12GENICpossibly homozygous46948927
186069861060698611TC15GENICpossibly homozygous46480000
186069893860698939AC7GENIChomozygous46480001
186069894060698941CT7GENIChomozygous46480002
186069970060699701GA13GENIChomozygous46948928
186070066060700661AG28GENIChomozygous46480005
186070164060701641CA18GENICpossibly homozygous46948929
186070190060701901AC18GENICheterozygous46480008
186070239660702397TG15GENIChomozygous46948930
186070240660702407AG14GENIChomozygous46480009
186070246960702470TC10GENICheterozygous46480011