chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219348771219348772GT3GENIChomozygous108993877
1219349380219349381CA15GENIChomozygous108993878
1219350152219350153AT26GENIChomozygous108993879
1219350192219350193CG26GENIChomozygous108993880
1219350474219350475AC23GENIChomozygous108993881
1219351351219351352TC23GENIChomozygous108993882
1219352558219352559GA25GENIChomozygous108993883
1219352599219352600AC25GENIChomozygous108993884
1219352617219352618TC24GENIChomozygous108993885
1219352708219352709GA23GENIChomozygous108993886
1219354427219354428AG24GENIChomozygous108993887
1219355996219355997GC15GENIChomozygous108993888
1219356163219356164TC16GENIChomozygous108993889
1219357048219357049TC21GENIChomozygous108993890
1219357860219357861GC28GENICpossibly homozygous108993891
1219358448219358449TC21GENIChomozygous108993892
1219360054219360055GA23GENIChomozygous108993893
1219361551219361552AG23GENIChomozygous108993894
1219361768219361769TG22GENIChomozygous108540618