chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151380115151380116TC15GENIChomozygous112886010
4151388655151388656TC14GENIChomozygous112886012
4151391132151391133AC15GENIChomozygous112886013
4151391175151391176CT17GENIChomozygous112886014
4151391761151391762GA18GENIChomozygous112886015
4151394598151394599GA18GENIChomozygous112886016
4151395043151395044CT18GENIChomozygous112886017
4151395187151395188TC12GENIChomozygous112886018
4151395515151395516AG24GENIChomozygous112886019
4151395584151395592AACAGGGA18GENIChomozygous128091550
4151394223151394223C18GENIChomozygous128091549
4151395953151395954TC15GENIChomozygous112886020
4151396190151396191TA26GENIChomozygous112886021
4151396252151396253GT23GENIChomozygous112886022
4151396522151396523AG15GENICheterozygous131646271
4151396526151396536ACACACACAT14GENICheterozygous131642762
4151396579151396580GC14GENIChomozygous112886023
4151396536151396537AG16GENIChomozygous119626849
4151386009151386010G11GENIChomozygous128091546
4151391443151391447ACAC17GENIChomozygous128091547