chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188784534188784535AC46GENIChomozygous110169898
2188784880188784881AG25GENIChomozygous110169900
2188785795188785796GA21GENIChomozygous110169902
2188785815188785816CT23GENIChomozygous110169904
2188786514188786515CG28GENIChomozygous110169906
2188788584188788585GA13GENIChomozygous110169907
2188791004188791005TG22GENIChomozygous110169909
2188791231188791232CT20GENICpossibly homozygous110169913
2188791388188791389GT30GENIChomozygous110169915
2188791391188791392AG28GENIChomozygous110169916
2188791478188791479TC28GENIChomozygous110169918
2188792955188792956TC31GENIChomozygous110169920
2188793408188793409CT25GENIChomozygous110169921
2188793614188793615CT21GENIChomozygous110169923
2188793754188793755AG19GENIChomozygous110169925