chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110448744110448745CCA20GENICheterozygous57596033
3110450384110450385G-30GENIChomozygous57596042
3110450390110450391CCG30GENIChomozygous57596045
3110450394110450395G-29GENIChomozygous57596047
3110481604110481605CCTT12GENICpossibly homozygous58618775