chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161068796161068797T-22GENIChomozygous55817089
5161069082161069083AG41GENICpossibly homozygous55817090
5161069544161069545TA34GENIChomozygous55817091
5161069923161069924AACC17GENIChomozygous55817092
5161069932161069933CCCA15GENICheterozygous55817093
5161070675161070678CCT---35GENIChomozygous55817094
5161071246161071247CG39GENIChomozygous55817095
5161071298161071299CG40GENIChomozygous55817096
5161071962161071963TC43GENIChomozygous55817097
5161072125161072126CT44GENIChomozygous55817098
5161072348161072349CCT27GENICheterozygous55817099
5161072616161072617C-48GENIChomozygous55817100
5161072748161072749AG67GENIChomozygous55817101
5161072877161072878GA52GENIChomozygous55817102
5161073063161073064AT42GENIChomozygous55817103
5161073248161073249GT28GENIChomozygous55817104
5161073586161073587CT42GENIChomozygous55817105