chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4174231363174231364AG23GENIChomozygous57979400
4174231580174231581TA38GENICpossibly homozygous57979403
4174232086174232087TC21GENIChomozygous57979406
4174232248174232249GC22GENIChomozygous57979409
4174232722174232723GC33GENIChomozygous57979418
4174232902174232903AG37GENIChomozygous57979421
4174233079174233080CT21GENICpossibly homozygous57979427
4174233198174233199CA11GENIChomozygous58265581
4174233272174233273CA25GENIChomozygous57979436
4174233402174233403AC31GENIChomozygous57979439
4174233403174233404TC30GENIChomozygous57979442
4174233467174233468TC34GENIChomozygous57979445
4174233696174233697CCCTT27GENIChomozygous57979451
4174233776174233777TC31GENIChomozygous57979454