chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171796814317968144GA55GENIChomozygous796174020
171796841817968419CT44GENICpossibly homozygous796174021
171797053117970532TC43GENICpossibly homozygous796174022
171797325017973251AG30GENIChomozygous796174023
171797365017973651CT33GENIChomozygous796174024
171797477917974780TC30GENIChomozygous796174025
171797486817974869AC36GENIChomozygous796174026
171797520817975209AT56GENIChomozygous796174027
171797596217975963CT61GENIChomozygous796174028
171797674417976745CT40GENIChomozygous796174029
171797729417977295GA42GENIChomozygous796174030
171797954517979546GA53GENIChomozygous796174031
171798042217980423AG55GENICpossibly homozygous796174032
171798045517980456CT66GENIChomozygous796174033
171798152117981522CT49GENICpossibly homozygous796174034
171798257417982575AG66GENIChomozygous796174035
171798306917983070AG45GENIChomozygous796174036
171798420117984202AG59GENIChomozygous796174037
171798440217984403GA38GENICpossibly homozygous796174038
171798462917984630AT69GENICpossibly homozygous796174039
171798500017985001GA38GENIChomozygous796174040
171798569117985692AG49GENIChomozygous796174041
171798670717986708CT62GENIChomozygous796174042
171798775917987760GT37GENIChomozygous796174043