chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4046990340469904AG14GENIChomozygous108256752
X4056638240566383GT11GENIChomozygous108256774
X4056650540566506GA10GENIChomozygous108256777
X4056651340566514TA10GENIChomozygous108256779
X4056651540566516AT11GENICpossibly homozygous108256781
X4063166640631667TC6GENIChomozygous108256783
X4064524240645243TG5GENIChomozygous108256789
X4065928540659286CT5GENIChomozygous108608289
X4068493240684933CT11GENIChomozygous108256791
X4068493540684936CT11GENIChomozygous108256793
X4068731740687318TG12GENIChomozygous108256795
X4070348240703483GT14GENIChomozygous108256799
X4056782440567825CG3GENIChomozygous108446454
X4063202540632026CA10GENIChomozygous108446458
X4052633340526334AT6GENIChomozygous108380422
X4052633540526336AC6GENIChomozygous108380424