chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124339161124339162GC30GENIChomozygous947301554
7124339853124339854CT17GENIChomozygous947301555
7124340150124340151TC25GENIChomozygous947301556
7124340593124340594GT15GENIChomozygous947301557
7124341640124341641CT24GENIChomozygous947301558
7124342221124342222AG23GENIChomozygous947301559
7124342808124342809AG37GENIChomozygous947301560
7124343070124343071TC20GENIChomozygous947301561
7124344290124344291CA18GENIChomozygous947301562
7124344725124344726AG28GENIChomozygous947301563
7124346017124346018AG20GENIChomozygous947301564
7124346085124346086CT21GENIChomozygous947301565
7124346457124346458AC40GENIChomozygous947301566
7124346977124346978TC22GENIChomozygous947301567
7124347350124347351CT36GENIChomozygous947301568
7124349089124349090TG27GENIChomozygous947301569
7124349853124349854TC5GENIChomozygous947301570
7124350157124350158GA14GENIChomozygous947301571
7124350303124350304TC21GENIChomozygous947301572
7124350783124350784CT32GENIChomozygous947301573
7124351259124351260TG27GENIChomozygous947301574
7124351260124351261GC26GENIChomozygous947301575
7124351265124351266AG24GENIChomozygous947301576
7124354044124354045TC21GENIChomozygous947301577
7124354543124354544TC31GENIChomozygous947301578
7124355098124355099CT35GENIChomozygous947301579
7124355645124355646GA25GENIChomozygous947301580
7124356412124356413AG26GENIChomozygous947301581
7124357561124357562GC31GENIChomozygous947301582
7124357590124357591CT31GENIChomozygous947301583
7124360268124360269GA32GENIChomozygous947301584
7124360930124360931GA15GENIChomozygous947301585
7124364056124364057CT31GENIChomozygous947301586
7124364485124364486GA13GENIChomozygous947301587
7124364758124364759CT19GENIChomozygous947301588
7124365980124365981CT29GENIChomozygous947301589
7124366145124366146TC32GENIChomozygous947301590
7124366572124366573GA26GENIChomozygous947301591