chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142392695142392696GC32GENIChomozygous56960492
4142392718142392719TTTGA24GENIChomozygous56960493
4142393502142393504AA--16GENICpossibly homozygous58444503
4142394432142394433TC22GENIChomozygous56960495
4142395616142395617G-7GENIChomozygous58589613
4142395648142395649AG20GENIChomozygous56960498
4142396752142396753CT33GENIChomozygous56960500
4142397545142397546CT26GENIChomozygous56960501
4142399124142399125GC24GENIChomozygous56960502
4142399185142399189GTGT----9GENICheterozygous58467248
4142405088142405089TC30GENIChomozygous56960503
4142405810142405811A-23GENIChomozygous56960504
4142404249142404250A-13GENICheterozygous57504492
4142411520142411521CCA17GENICheterozygous58567644
4142413456142413457CT34GENIChomozygous56960505
4142415536142415537GT20GENIChomozygous56960506
4142415551142415552CT17GENIChomozygous56960507
4142408808142408820GTGTGTGTGTGC------------19GENICpossibly homozygous58659565