chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4174231363174231364AG30GENICpossibly homozygous57979400
4174231580174231581TA23GENICpossibly homozygous57979403
4174231668174231669CT33GENICpossibly homozygous58357068
4174231669174231670TC34GENICpossibly homozygous58357070
4174232086174232087TC24GENIChomozygous57979406
4174232248174232249GC23GENIChomozygous57979409
4174232722174232723GC32GENIChomozygous57979418
4174232902174232903AG33GENIChomozygous57979421
4174233079174233080CT41GENICpossibly homozygous57979427
4174233198174233199CA40GENIChomozygous58265581
4174233272174233273CA32GENIChomozygous57979436
4174233402174233403AC29GENIChomozygous57979439
4174233403174233404TC29GENIChomozygous57979442
4174233467174233468TC37GENIChomozygous57979445
4174233696174233697CCCTT24GENIChomozygous57979451
4174233776174233777TC17GENIChomozygous57979454