chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109201856492018565TC24GENIChomozygous973384748
109201857992018580CG27GENIChomozygous973384749
109201876892018769TG15GENIChomozygous973384750
109201887892018879GT20GENIChomozygous973384751
109201939292019393CA17GENIChomozygous973384752
109201973392019734GA10GENIChomozygous973384753
109201980592019806AG13GENIChomozygous973384754
109201999192019992CT12GENIChomozygous973384755
109202014492020145AG11GENIChomozygous973384756
109202043492020435AG17GENIChomozygous973384757
109202046192020462CG16GENIChomozygous973384758
109202066792020668TC24GENIChomozygous973384759
109202102492021025TC22GENIChomozygous973384760
109202105992021060AG23GENIChomozygous973384761
109202137592021376TC20GENIChomozygous973384762
109202169992021700CT27GENIChomozygous973384763
109202206192022062AG15GENIChomozygous973384764
109202212792022128TG21GENIChomozygous973384765
109202251292022513GT21GENIChomozygous973384766
109202325092023251CT14GENIChomozygous973384767
109202361992023620AG9GENIChomozygous973384768
109202558792025588GA25GENICpossibly homozygous973384769
109202805992028060TA13GENIChomozygous973384770
109202976992029770AG19GENIChomozygous973384771
109203153792031538GC21GENIChomozygous973384772
109203414092034141CG18GENIChomozygous973384773
109203533192035332CG19GENIChomozygous973384774
109203712092037121CT13GENIChomozygous973384775
109203751992037520TC15GENIChomozygous973384776
109203954092039541GT29GENIChomozygous973384777
109203958092039581CG29GENIChomozygous973384778
109203984392039844TC20GENIChomozygous973384779