chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67562730375627304CA28GENIChomozygous114861627
67562753475627535CG21GENIChomozygous114861628
67562784475627845AG23GENIChomozygous114861629
67562889375628894AG14GENIChomozygous114861630
67562994775629948TA27GENIChomozygous114861631
67563011175630112CT21GENIChomozygous114861632
67563084175630842AG26GENIChomozygous114861634
67563342675633427CT12GENIChomozygous114861635
67563361375633614CA26GENIChomozygous114861636
67563390975633910CG24GENIChomozygous114861637
67563409675634097AG17GENIChomozygous114861638
67563471575634716GC41GENIChomozygous114861639
67563534375635344TC35GENIChomozygous114861640
67563592675635927CT20GENIChomozygous114861641
67563623275636233CG30GENIChomozygous114861642
67564129875641299TA28GENIChomozygous114861644
67564131675641317TC30GENIChomozygous114861645
67564486775644868CT27GENIChomozygous114861646
67564571075645711TC17GENIChomozygous114861647
67564579475645795AT23GENIChomozygous114861648
67564647175646472TC26GENIChomozygous114861649
67564789275647893GA37GENIChomozygous114861650
67565038775650388AT21GENIChomozygous114861651
67565264375652644TC20GENIChomozygous114861653
67565581775655818CT15GENIChomozygous114861658
67565584275655843CT24GENIChomozygous114861659
67565649875656499CG12GENIChomozygous114861660
67565779075657791CT30GENIChomozygous114861661
67566212875662129GA21GENIChomozygous114861662
67566288575662886TC31GENIChomozygous114861663
67566771975667720AT36GENIChomozygous114861664
67566862275668623CT17GENIChomozygous114861665
67567013875670139CT5GENIChomozygous114861666