chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161499680161499681GGC44GENIChomozygous55818570
5161499812161499813CG27GENIChomozygous55818571
5161500148161500149CCTT14GENIChomozygous55818572
5161501726161501727CT18GENIChomozygous55818573
5161502106161502107A-16GENIChomozygous55818574
5161503285161503286AAT18GENICpossibly homozygous55818575
5161506346161506347AG29GENIChomozygous55818576
5161506779161506780GC17GENIChomozygous55818577