chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151380115151380116TC17GENIChomozygous112886010
4151388655151388656TC14GENIChomozygous112886012
4151391132151391133AC13GENIChomozygous112886013
4151391175151391176CT21GENIChomozygous112886014
4151391446151391447CT11GENICheterozygous126054221
4151391761151391762GA20GENIChomozygous112886015
4151394598151394599GA23GENIChomozygous112886016
4151395043151395044CT13GENIChomozygous112886017
4151395187151395188TC7GENIChomozygous112886018
4151395515151395516AG19GENIChomozygous112886019
4151395953151395954TC22GENIChomozygous112886020
4151396190151396191TA12GENIChomozygous112886021
4151396252151396253GT17GENIChomozygous112886022
4151396579151396580GC12GENIChomozygous112886023