chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197325134197326GC17GENIChomozygous114015926
5134197335134197336AC21GENIChomozygous114015927
5134197339134197340AG23GENIChomozygous114015928
5134197402134197403GA31GENIChomozygous114015929
5134197868134197869AT13GENIChomozygous114015931
5134199793134199794TC16GENIChomozygous114015938
5134200267134200268GA16GENIChomozygous114015939
5134201380134201381GT25GENICpossibly homozygous114015941
5134202316134202317TG22GENIChomozygous114015942
5134203256134203257AC20GENIChomozygous114015943
5134206183134206184AT24GENICheterozygous114015955
5134206188134206189CT24GENICheterozygous114015956
5134206205134206206GC22GENICheterozygous114015957
5134206206134206207GC22GENICheterozygous114015958
5134206221134206222GA28GENICheterozygous118858430
5134206223134206224AG27GENICheterozygous118858431
5134206440134206441GT47GENICheterozygous114015963
5134206476134206477AG44GENICheterozygous114015964
5134206615134206616CT35GENICheterozygous114015965
5134206617134206618GT34GENICheterozygous114015966
5134206707134206708CT35GENICheterozygous114015967
5134206744134206745AG48GENICheterozygous114015968
5134206769134206770GA47GENICheterozygous114015969
5134206790134206791AG46GENICheterozygous114015970
5134206887134206888GA52GENICheterozygous114015971