chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184339184184340AATC13GENICpossibly homozygous61313321
1184184349184184350CCTA13GENICheterozygous62272678
1184184618184184619GA31GENIChomozygous61567047
1184184394184184395CT21GENIChomozygous60998679
1184185916184185920TTTC----21GENIChomozygous61567048
1184185935184185936TC28GENIChomozygous60998683
1184185964184185967TTT---18GENIChomozygous61567050
1184186294184186295GA17GENIChomozygous60998686
1184186369184186374CCGCC-----17GENIChomozygous60998688
1184186433184186434TC16GENIChomozygous60998689
1184187251184187252T-13GENIChomozygous61567051
1184188059184188060CT22GENIChomozygous60998692
1184188545184188546GGT38GENIChomozygous60998693
1184188885184188886CCAGAGAGAGGCAGAGACAGAAAG5GENIChomozygous62272679