chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148182137981821379TCTAATGGCAGTG65GENIChomozygous131730557
148182138181821381T64GENIChomozygous131730558
148182167481821675CA69GENIChomozygous114098595
148182172481821725TC79GENICpossibly homozygous114098596
148182469081824691CG68GENIChomozygous114098597
148182545281825453TC58GENIChomozygous114098598
148182577081825771CG70GENIChomozygous114098599
148182598481825985AG65GENIChomozygous114098600
148182632781826327G64GENIChomozygous131730559
148182727481827275TC59GENIChomozygous114098601
148182753581827536AG44GENIChomozygous114098602
148182980781829808AT55GENIChomozygous114098603
148182986681829867TA60GENICpossibly homozygous114098604
148183082481830824AGGAAAAGG28GENIChomozygous131730560
148183245181832452GA76GENIChomozygous114098605
148183338881833389CT66GENIChomozygous114098606