chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197078134197079CT23GENIChomozygous975770031
5134197761134197762TA29GENIChomozygous975770032
5134199531134199532TG27GENIChomozygous975770033
5134201404134201405GA14GENIChomozygous975770034
5134203699134203700CT29GENIChomozygous975770035
5134206183134206184AT41GENICheterozygous975770036
5134206188134206189CT42GENICheterozygous975770037
5134206205134206206GC47GENICheterozygous975770038
5134206206134206207GC47GENICheterozygous975770039
5134206221134206222GA49GENICheterozygous975770040
5134206223134206224AG52GENICheterozygous975770041
5134206283134206284TG38GENICheterozygous975770042
5134206351134206352AG39GENICheterozygous975770043
5134206406134206407TG56GENICheterozygous975770044
5134206440134206441GT63GENICheterozygous975770045
5134206615134206616CT44GENICheterozygous975770046
5134206617134206618GT42GENICheterozygous975770047
5134206707134206708CT57GENICheterozygous975770048
5134206744134206745AG67GENICheterozygous975770049
5134206769134206770GA73GENICheterozygous975770050
5134206790134206791AG79GENICheterozygous975770051