chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218121773218121774GGT18GENIChomozygous61087037
1218122448218122449TTGGG3GENIChomozygous61087040
1218122478218122479TA12GENIChomozygous61087041
1218122479218122480TTAC12GENIChomozygous61087042
1218123107218123108GA50GENIChomozygous61087043
1218125442218125443AG25GENIChomozygous61087045
1218126897218126909ACACACACACAC------------8GENICheterozygous62198920
1218126901218126909ACACACAC--------8GENICpossibly homozygous62198922
1218127200218127201TC30GENIChomozygous61087046
1218127523218127524TTAC10GENICpossibly homozygous61087047
1218127552218127553GA20GENIChomozygous61087049
1218131751218131752GA34GENIChomozygous61087050
1218131792218131793AG36GENIChomozygous61087051