chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110446939110446940CT21GENIChomozygous57984261
3110447485110447486TG19GENIChomozygous57596021
3110448235110448238AAA---17GENIChomozygous57596024
3110448744110448745CCAA12GENICheterozygous57596030
3110448744110448745CCA12GENICpossibly homozygous57596033
3110448784110448785AG15GENIChomozygous57984264
3110449926110449927AG26GENIChomozygous57596036
3110450013110450014CA33GENIChomozygous57596039
3110450384110450385G-12GENIChomozygous57596042
3110450390110450391CCG12GENIChomozygous57596045
3110450394110450395G-11GENIChomozygous57596047