chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104531905145319052A-2GENIChomozygous51442210
104531948845319489CG16GENIChomozygous51873363
104532031145320312TTATGG6GENIChomozygous51873366
104532169545321696TC23GENICpossibly homozygous51873369
104532171145321712AC21GENIChomozygous51873372
104532252245322523AG11GENIChomozygous51873375
104532417045324171TTACTC6GENIChomozygous51442213
104532434745324348AG2GENIChomozygous52317951
104532436045324362CA--3GENICheterozygous51873381
104532450845324509CT32GENICpossibly homozygous51873384
104532507245325075GGT---7GENIChomozygous51442216
104532664345326644A-11GENIChomozygous51873387
104532723045327231AG25GENIChomozygous51873390
104532913945329140CT32GENICpossibly homozygous51442220
104533007745330078CT29GENICpossibly homozygous51873396
104533054345330544A-4GENICheterozygous51442221
104533061845330619CCTGT2GENICheterozygous51873399
104533139645331397AC30GENIChomozygous51873402
104533362745333628GGTAGCTAGC1GENIChomozygous51442227