chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6100291857100291858T4GENIChomozygous137700512
6100295567100295568TG19GENIChomozygous137862686
6100295736100295737CG11GENIChomozygous137862687
6100300469100300470GA25GENIChomozygous141853170
6100300786100300787CT20GENIChomozygous141853171
6100303302100303303AG14GENIChomozygous137862689
6100305860100305863TCC3GENIChomozygous137700515
6100307874100307875GA17GENIChomozygous141853172
6100308344100308345GT17GENIChomozygous141853173
6100311210100311211TC17GENIChomozygous141853174
6100318430100318431T19GENIChomozygous137700517
6100318679100318679TGTGTA15GENICpossibly homozygous137700518
6100320701100320702TA13GENIChomozygous137862692
6100320932100320933TC15GENIChomozygous137862693
6100321626100321627TC16GENIChomozygous137862694
6100322838100322839CT17GENIChomozygous141853175
6100324939100324940GT23GENIChomozygous141853176
6100325482100325483CT20GENIChomozygous141853177
6100325993100325994AG11GENIChomozygous137862697
6100328021100328022CT19GENIChomozygous141853178
6100328257100328258TG13GENIChomozygous137862698
6100318681100318681TGTA16GENICheterozygous144749691
6100308521100308525AAAT18GENIChomozygous141785419
6100325395100325396G18GENIChomozygous141785420
6100328685100328686GA15GENIChomozygous137862699