chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178088301480883015GA16GENIChomozygous111112251
178088330780883308GC21GENIChomozygous111112253
178088373180883732TG15GENIChomozygous111112255
178088428180884282CT26GENIChomozygous111112257
178088492580884926CT32GENIChomozygous111112259
178088500880885009TA28GENIChomozygous111112261
178088506580885066AC29GENIChomozygous111112263
178088563680885637GA19GENIChomozygous111112265
178088595680885957CT24GENICpossibly homozygous111112267
178088607180886072GA18GENIChomozygous111112269
178088621180886212CT21GENIChomozygous111112271
178088638580886386TC15GENIChomozygous111112273
178088642480886425CT15GENIChomozygous111112275
178088809080888091CT46GENIChomozygous111112277
178088897180888972AG18GENIChomozygous111112279
178088897480888975GA20GENIChomozygous111112281
178088924280889243AC24GENIChomozygous111112283
178088976680889767AG27GENIChomozygous111112287
178089077080890771CT26GENIChomozygous111112289
178088798580887986AT58GENICpossibly homozygous111217655