chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110446939110446940CT29GENIChomozygous57984261
3110447485110447486TG22GENIChomozygous57596021
3110448235110448238AAA---24GENIChomozygous57596024
3110448744110448745CCAA14GENICheterozygous57596030
3110448744110448745CCA14GENICpossibly homozygous57596033
3110448784110448785AG29GENIChomozygous57984264
3110449926110449927AG35GENIChomozygous57596036
3110450013110450014CA28GENIChomozygous57596039
3110450384110450385G-21GENIChomozygous57596042
3110450390110450391CCG24GENIChomozygous57596045
3110450394110450395G-24GENIChomozygous57596047