chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141506153215061533TC22GENIChomozygous113355995
141506172715061728TC14GENIChomozygous113355997
141506760315067604CT24GENIChomozygous113355999
141508251515082516GC35GENIChomozygous113356001
141508589015085891CT19GENIChomozygous113356003
141509393315093934AG12GENIChomozygous113356005
141510388515103886TG12GENICheterozygous113356007
141510446715104468GC28GENIChomozygous113660761
141510483515104836AC40GENIChomozygous113356009
141510505915105060CT32GENIChomozygous113356011
141510714815107149TA18GENIChomozygous113356013
141512596915125970GT9GENIChomozygous113576146
141512623115126232TG11GENIChomozygous113356019
141512644615126447TG16GENIChomozygous113356021
141512872715128728TG21GENIChomozygous113356023
141513157515131576AG38GENIChomozygous113356025
141513213415132135GA23GENIChomozygous113356027
141514215015142151CT20GENIChomozygous113356029
141514393215143933TC40GENIChomozygous113356031
141514405315144054AG40GENIChomozygous113356033
141514680915146810GA37GENIChomozygous113356035
141514696915146970AG32GENIChomozygous113356037