chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4174231363174231364AG12GENIChomozygous57979400
4174231580174231581TA19GENICpossibly homozygous57979403
4174231668174231669CT15GENICheterozygous58357068
4174231669174231670TC15GENICheterozygous58357070
4174232086174232087TC18GENICpossibly homozygous57979406
4174232248174232249GC17GENICpossibly homozygous57979409
4174232722174232723GC12GENIChomozygous57979418
4174232902174232903AG7GENICheterozygous57979421
4174233079174233080CT20GENIChomozygous57979427
4174233198174233199CA17GENICpossibly homozygous58265581
4174233272174233273CA20GENIChomozygous57979436
4174233402174233403AC8GENICpossibly homozygous57979439
4174233403174233404TC9GENICpossibly homozygous57979442
4174233467174233468TC18GENIChomozygous57979445
4174233696174233697CCCTT8GENIChomozygous57979451
4174233776174233777TC20GENICpossibly homozygous57979454