chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147250798147250799GA13GENIChomozygous114045349
5147251047147251048TC26GENIChomozygous114045351
5147252430147252431AG6GENIChomozygous126205855
5147253389147253390CG12GENIChomozygous114045355
5147253494147253495AG8GENIChomozygous114045357
5147253845147253846TC18GENIChomozygous114045359
5147254148147254149AT11GENIChomozygous114045361
5147254281147254282GA19GENIChomozygous114045363
5147256451147256452TC17GENIChomozygous114045367
5147257281147257282AG17GENIChomozygous114045369
5147258180147258181AG19GENIChomozygous114045371
5147258227147258228TC7GENIChomozygous114152750
5147258807147258808CG12GENIChomozygous114045373
5147259500147259501GA17GENIChomozygous114045375
5147259569147259570AG27GENIChomozygous114045377
5147259907147259908CT19GENIChomozygous114045379
5147262075147262076TG8GENIChomozygous114045381
5147262321147262322CT4GENIChomozygous114045383
5147262797147262798GT10GENICheterozygous114045385
5147263917147263918CG16GENIChomozygous114045387
5147264273147264274GA25GENIChomozygous114045389
5147265058147265059GA22GENIChomozygous114045391
5147265083147265084CG29GENIChomozygous114045393
5147265621147265622CT5GENIChomozygous114045399
5147265931147265932TC18GENIChomozygous114045401
5147268241147268242AG8GENIChomozygous114045403
5147268277147268278GA17GENIChomozygous114045405
5147268743147268744CT10GENIChomozygous114045407