chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4174231363174231364AG20GENIChomozygous57979400
4174231580174231581TA23GENICpossibly homozygous57979403
4174231668174231669CT26GENIChomozygous58357068
4174231669174231670TC26GENIChomozygous58357070
4174232086174232087TC15GENIChomozygous57979406
4174232248174232249GC19GENIChomozygous57979409
4174232722174232723GC20GENIChomozygous57979418
4174232902174232903AG26GENIChomozygous57979421
4174233079174233080CT20GENIChomozygous57979427
4174233198174233199CA21GENIChomozygous58265581
4174233272174233273CA24GENIChomozygous57979436
4174233402174233403AC35GENIChomozygous57979439
4174233403174233404TC36GENIChomozygous57979442
4174233467174233468TC23GENIChomozygous57979445
4174233696174233697CCCTT17GENIChomozygous57979451
4174233776174233777TC18GENIChomozygous57979454