chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151380115151380116TC32GENIChomozygous112886010
4151388655151388656TC27GENIChomozygous112886012
4151391132151391133AC26GENIChomozygous112886013
4151391175151391176CT19GENIChomozygous112886014
4151391761151391762GA19GENIChomozygous112886015
4151394223151394223C31GENIChomozygous128091549
4151386009151386010G25GENIChomozygous128091546
4151391443151391447ACAC20GENIChomozygous128091547
4151393056151393056AGGGGA9GENICpossibly homozygous128091548
4151394598151394599GA27GENIChomozygous112886016
4151395043151395044CT29GENIChomozygous112886017
4151395187151395188TC30GENIChomozygous112886018
4151395515151395516AG19GENIChomozygous112886019
4151395584151395592AACAGGGA20GENIChomozygous128091550
4151395953151395954TC24GENIChomozygous112886020
4151396190151396191TA23GENIChomozygous112886021
4151396252151396253GT26GENIChomozygous112886022
4151396522151396523AG25GENICheterozygous131646271
4151396526151396536ACACACACAT25GENICheterozygous131642762
4151396579151396580GC31GENIChomozygous112886023
4151396536151396537AG30GENIChomozygous119626849