chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218121773218121774GGT21GENICpossibly homozygous61087037
1218122448218122449TTGGG1GENIChomozygous61087040
1218122478218122479TA4GENIChomozygous61087041
1218122479218122480TTAC4GENIChomozygous61087042
1218123107218123108GA24GENIChomozygous61087043
1218125442218125443AG11GENIChomozygous61087045
1218126901218126909ACACACAC--------3GENIChomozygous62198922
1218127200218127201TC12GENIChomozygous61087046
1218127523218127524TTAC1GENIChomozygous61087047
1218127552218127553GA4GENIChomozygous61087049
1218131751218131752GA15GENIChomozygous61087050
1218131792218131793AG16GENIChomozygous61087051