chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101022050101022050ACAA57GENIChomozygous128217990
5101058281101058281T43GENIChomozygous128218017
5101058285101058285T46GENIChomozygous128218018
5101058290101058290A44GENIChomozygous128218019
5101058295101058295A44GENIChomozygous128218020
5101058379101058380C61GENIChomozygous128218021
5101058388101058389C64GENIChomozygous128218022
5101141283101141283TG25GENIChomozygous128218059
5101144159101144161TG37GENICheterozygous130655038
5101058291101058292GT44GENIChomozygous118844446
5101074252101074253TA23GENIChomozygous114131768
5101074253101074254CT23GENIChomozygous114131769
5101117311101117311GC51GENICpossibly homozygous132077682