chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142244801142244802CT21GENIChomozygous115941604
7142245679142245680GA22GENIChomozygous115941605
7142247107142247108GA22GENIChomozygous115941606
7142248012142248013CT21GENIChomozygous115941607
7142252185142252186GA11GENIChomozygous115941614
7142252513142252514GT17GENIChomozygous115941615
7142253909142253910GA10GENIChomozygous115941617
7142253931142253932AG12GENIChomozygous115941618
7142254186142254187TC25GENIChomozygous115941619
7142254253142254254GA24GENIChomozygous115941620
7142256275142256276TC26GENIChomozygous115941622
7142256367142256368TC19GENIChomozygous115941623
7142256512142256513TC20GENIChomozygous115941624
7142256533142256534AG14GENIChomozygous115941625
7142257293142257294TG27GENIChomozygous115941626
7142257429142257430AT18GENIChomozygous115941627
7142257603142257604TC3GENICheterozygous115941628
7142258013142258014TC6GENIChomozygous115941629
7142258559142258560CT22GENIChomozygous115941630
7142260650142260651GA13GENIChomozygous115941631