chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184023575140235752GGA22GENIChomozygous46426585
184023600540236006AAT19GENICpossibly homozygous46426586
184023662240236623T-16GENIChomozygous46426587
184023721140237212TA23GENIChomozygous46426588
184023733940237340TC29GENIChomozygous46426589
184023743340237434GT36GENIChomozygous46426590
184024032140240322CT19GENIChomozygous46426592
184024075240240753GA19GENIChomozygous46426593
184024080740240808CG22GENIChomozygous46426594