chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184339184184340AATC14GENICpossibly homozygous61313321
1184184618184184619GA16GENIChomozygous61567047
1184185916184185920TTTC----27GENIChomozygous61567048
1184184349184184350CCTA11GENICheterozygous62272678
1184184394184184395CT18GENIChomozygous60998679
1184185935184185936TC28GENIChomozygous60998683
1184185964184185967TTT---27GENIChomozygous61567050
1184186294184186295GA22GENIChomozygous60998686
1184186369184186374CCGCC-----15GENIChomozygous60998688
1184186433184186434TC21GENIChomozygous60998689
1184187251184187252T-23GENIChomozygous61567051
1184187377184187385TTTTTTTT--------1GENIChomozygous62313765
1184188059184188060CT26GENIChomozygous60998692
1184188545184188546GGT16GENIChomozygous60998693
1184188885184188886CCAGAGAGAGGCAGAGACAGAAAG9GENICpossibly homozygous62272679