chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197078134197079CT22GENIChomozygous961043718
5134201404134201405GA18GENIChomozygous961043719
5134202316134202317TG22GENIChomozygous961043720
5134203699134203700CT17GENIChomozygous961043721
5134206183134206184AT42GENICheterozygous961043722
5134206188134206189CT43GENICheterozygous961043723
5134206205134206206GC42GENICheterozygous961043724
5134206206134206207GC40GENICheterozygous961043725
5134206221134206222GA41GENICheterozygous961043726
5134206223134206224AG41GENICheterozygous961043727
5134206406134206407TG26GENICheterozygous961043728
5134206440134206441GT31GENICheterozygous961043729
5134206707134206708CT43GENICheterozygous961043730
5134206744134206745AG41GENICheterozygous961043731
5134206769134206770GA39GENICheterozygous961043732
5134206790134206791AG39GENICheterozygous961043733