chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184023575140235752GGA33GENICpossibly homozygous46426585
184023600540236006AAT17GENIChomozygous46426586
184023662240236623T-18GENIChomozygous46426587
184023721140237212TA30GENIChomozygous46426588
184023733940237340TC21GENIChomozygous46426589
184023743340237434GT34GENIChomozygous46426590
184024032140240322CT28GENIChomozygous46426592
184024075240240753GA9GENIChomozygous46426593
184024080740240808CG17GENIChomozygous46426594