chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184184339184184340AATC9GENICpossibly homozygous61313321
1184184618184184619GA36GENIChomozygous61567047
1184185916184185920TTTC----30GENIChomozygous61567048
1184184349184184350CCTA8GENICpossibly homozygous62272678
1184184394184184395CT22GENIChomozygous60998679
1184185935184185936TC32GENIChomozygous60998683
1184185964184185967TTT---23GENIChomozygous61567050
1184186294184186295GA31GENIChomozygous60998686
1184186369184186374CCGCC-----15GENIChomozygous60998688
1184186433184186434TC12GENIChomozygous60998689
1184187251184187252T-23GENIChomozygous61567051
1184187377184187385TTTTTTTT--------8GENICheterozygous62313765
1184187378184187385TTTTTTT-------8GENICheterozygous62181554
1184188059184188060CT31GENIChomozygous60998692
1184188545184188546GGT17GENIChomozygous60998693
1184188885184188886CCAGAGAGAGGCAGAGACAGAAAG4GENIChomozygous62272679