chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176764777176764778GT22GENIChomozygous55849647
5176766615176766616CCTTT11GENICheterozygous56497436
5176766616176766618TT--11GENICpossibly homozygous56101434
5176766641176766642T-16GENIChomozygous56101436
5176767369176767370GA19GENIChomozygous55849651
5176767944176767945GC15GENIChomozygous56101438
5176768073176768074AT30GENIChomozygous56101440
5176768124176768125AG22GENIChomozygous55849653
5176768364176768365CT31GENIChomozygous56101442