chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184339184184340AATC20GENICpossibly homozygous61313321
1184184349184184350CCTA16GENICheterozygous62272678
1184184394184184395CT33GENIChomozygous60998679
1184184618184184619GA30GENIChomozygous61567047
1184185916184185920TTTC----23GENIChomozygous61567048
1184185935184185936TC26GENIChomozygous60998683
1184185964184185967TTT---19GENIChomozygous61567050
1184186294184186295GA25GENIChomozygous60998686
1184186369184186374CCGCC-----11GENIChomozygous60998688
1184186433184186434TC24GENIChomozygous60998689
1184187251184187252T-21GENIChomozygous61567051
1184187377184187385TTTTTTTT--------12GENICheterozygous62313765
1184187378184187385TTTTTTT-------12GENICheterozygous62181554
1184188059184188060CT37GENIChomozygous60998692
1184188545184188546GGT18GENIChomozygous60998693
1184188885184188886CCAGAGAGAGGCAGAGACAGAAAG6GENIChomozygous62272679