chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2206998689206998690CG12GENIChomozygous110216649
2207000844207000845CT20GENIChomozygous110216650
2207001852207001853TA29GENIChomozygous110216651
2207002092207002093TC21GENIChomozygous110216652
2207003782207003783GT16GENICpossibly homozygous110216653
2207004307207004308AG9GENIChomozygous110216654
2207006184207006185TC26GENIChomozygous110216655
2207006866207006867GA25GENIChomozygous110216656
2207007573207007574GA19GENICpossibly homozygous110216657