chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143327156143327157GA31GENIChomozygous57507369
4143327633143327634GA30GENIChomozygous57507371
4143327733143327734GC21GENIChomozygous57507373
4143327825143327826TC28GENIChomozygous57507375
4143327867143327868CT27GENIChomozygous57507377
4143328107143328108AG28GENICpossibly homozygous57507379
4143328108143328109CG28GENICpossibly homozygous57507381
4143328109143328110CT28GENICpossibly homozygous57507383
4143328147143328148GA17GENICpossibly homozygous57507385
4143328775143328776AC23GENICpossibly homozygous57507389
4143330445143330446GA17GENIChomozygous58082961