chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184339184184340AATC10GENICpossibly homozygous61313321
1184184618184184619GA24GENIChomozygous61567047
1184185916184185920TTTC----18GENICpossibly homozygous61567048
1184184349184184350CCTA7GENICheterozygous62272678
1184185935184185936TC18GENIChomozygous60998683
1184184394184184395CT18GENIChomozygous60998679
1184185964184185967TTT---16GENIChomozygous61567050
1184186294184186295GA19GENIChomozygous60998686
1184186369184186374CCGCC-----12GENIChomozygous60998688
1184186433184186434TC12GENIChomozygous60998689
1184187251184187252T-23GENIChomozygous61567051
1184187377184187385TTTTTTTT--------7GENICheterozygous62313765
1184187378184187385TTTTTTT-------7GENICheterozygous62181554
1184188059184188060CT24GENIChomozygous60998692
1184188545184188546GGT29GENICpossibly homozygous60998693
1184188885184188886CCAGAGAGAGGCAGAGACAGAAAG7GENIChomozygous62272679