chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171015455710154558CT33GENIChomozygous110953835
171015542410155425TA39GENIChomozygous110953837
171015705110157052TC35GENIChomozygous110953839
171015766610157667CT53GENIChomozygous110953841
171015788810157889TC58GENIChomozygous110953844
171015937610159377CG51GENIChomozygous110953846
171015991010159911AG46GENIChomozygous110953848
171016199710161998GA32GENIChomozygous110953850
171016327110163272AG55GENIChomozygous110953852
171016645010166451TG38GENIChomozygous110953854
171016645110166452CA37GENIChomozygous110953856
171016690110166902TC61GENIChomozygous110953858
171016722010167221AG45GENIChomozygous110953860
171016902610169027GC37GENIChomozygous110953862
171016921810169219AG18GENIChomozygous110953864
171016948310169484TG56GENIChomozygous110953866
171017000910170010TC47GENIChomozygous110953868
171017062110170622AG56GENIChomozygous110953870
171017163610171637AG45GENIChomozygous110953872
171017368410173685AG36GENIChomozygous110953874
171017414410174145TC31GENIChomozygous110953876
171017782610177827GA47GENIChomozygous110953878
171017994410179945GA18GENIChomozygous110953880
171018156010181561GA43GENIChomozygous110953882
171018169710181698AC33GENIChomozygous110953884
171018328310183284TC29GENIChomozygous110953886
171018359410183595GA34GENIChomozygous110953888
171018387610183877AG51GENIChomozygous110953890
171018422510184226CT34GENIChomozygous110953893
171018469010184691GA39GENIChomozygous110953895
171018501510185016CT42GENIChomozygous110953897
171018579310185794GA41GENIChomozygous110953900
171018650410186505AT41GENIChomozygous110953902
171018654810186549CA38GENIChomozygous110953904