chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143327156143327157GA20GENIChomozygous57507369
4143327633143327634GA10GENIChomozygous57507371
4143327733143327734GC15GENIChomozygous57507373
4143327825143327826TC22GENIChomozygous57507375
4143327867143327868CT14GENIChomozygous57507377
4143328107143328108AG15GENICpossibly homozygous57507379
4143328108143328109CG15GENICpossibly homozygous57507381
4143328109143328110CT16GENICpossibly homozygous57507383
4143328147143328148GA18GENIChomozygous57507385
4143328775143328776AC22GENIChomozygous57507389
4143330445143330446GA19GENIChomozygous58082961