chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197078134197079CT17GENIChomozygous114143770
5134197761134197762TA28GENICpossibly homozygous114143771
5134200267134200268GA24GENIChomozygous114015939
5134201404134201405GA13GENIChomozygous114143773
5134203699134203700CT29GENIChomozygous114143774
5134206221134206222GA57GENICheterozygous118858430
5134206223134206224AG59GENICheterozygous118858431
5134206406134206407TG54GENICheterozygous114015962
5134206440134206441GT64GENICheterozygous114015963
5134206476134206477AG48GENICheterozygous114015964
5134206615134206616CT40GENICheterozygous114015965
5134206617134206618GT41GENICheterozygous114015966
5134206707134206708CT59GENICheterozygous114015967
5134206744134206745AG54GENICheterozygous114015968
5134206769134206770GA61GENICheterozygous114015969
5134206790134206791AG52GENICheterozygous114015970