chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2034101573410158CG27GENICheterozygous63327572
2034106543410655AG35GENICpossibly homozygous63327587
2034110773411078CT96GENICheterozygous63327595
2034110793411080CG91GENICheterozygous63327597
2034111043411105GC70GENICheterozygous63327599
2034111313411132TC47GENICheterozygous63327600
2034130303413031AG53GENICheterozygous63327632