chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101391406613914067CT4GENIChomozygous116736542
101391445413914455TC4GENIChomozygous116736543
101391451613914517TG3GENIChomozygous116736544
101391740113917402GA7GENIChomozygous116736545
101391991013919911TG4GENIChomozygous117408006
101391993013919931CT2GENIChomozygous116736546
101392013113920132CA3GENIChomozygous116736547
101392181613921817TC4GENIChomozygous116736548
101392619913926200AT5GENIChomozygous116736551
101392635613926357CT3GENIChomozygous116736552
101393100913931010TC12GENIChomozygous116736553
101393478313934784AG6GENIChomozygous116736554
101393538913935390AG5GENIChomozygous116736555
101393557213935573GA5GENIChomozygous116736556
101393886913938870TC5GENIChomozygous116736557
101394116013941161AG12GENIChomozygous116736558
101394789013947891AG5GENIChomozygous116736559
101394800013948001TC8GENIChomozygous116736560
101394800713948008AC9GENIChomozygous116736561
101395120513951206CT3GENICheterozygous116736562
101395123513951236CT3GENICheterozygous117408008
101395123713951238CT3GENICheterozygous117408010
101395123913951240CT3GENICheterozygous117408012
101395142613951427AG3GENIChomozygous116736563
101395699613956997TC4GENIChomozygous116736564
101395786913957870GC6GENIChomozygous116736565