chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124339161124339162GC30GENIChomozygous115865589
7124339853124339854CT17GENIChomozygous115865591
7124340150124340151TC25GENIChomozygous116226616
7124340593124340594GT15GENIChomozygous116226617
7124341640124341641CT24GENIChomozygous116226618
7124342221124342222AG23GENIChomozygous116226619
7124342808124342809AG37GENIChomozygous116226620
7124343070124343071TC20GENIChomozygous116226621
7124344290124344291CA18GENIChomozygous115865605
7124344725124344726AG28GENIChomozygous116226622
7124346017124346018AG20GENIChomozygous115865615
7124346085124346086CT21GENIChomozygous116226624
7124346457124346458AC40GENIChomozygous116226625
7124346977124346978TC22GENIChomozygous115865617
7124347350124347351CT36GENIChomozygous116226626
7124349089124349090TG27GENIChomozygous115865623
7124349853124349854TC5GENIChomozygous116226627
7124350157124350158GA14GENIChomozygous116226628
7124350303124350304TC21GENIChomozygous116226629
7124350783124350784CT32GENIChomozygous116226630
7124351259124351260TG27GENIChomozygous118259334
7124351260124351261GC26GENIChomozygous118259336
7124351265124351266AG24GENIChomozygous115865627
7124354044124354045TC21GENIChomozygous115865631
7124354543124354544TC31GENIChomozygous115865633
7124355098124355099CT35GENIChomozygous116226631
7124355645124355646GA25GENIChomozygous116226632
7124356412124356413AG26GENIChomozygous116226633
7124357561124357562GC31GENIChomozygous116226635
7124357590124357591CT31GENIChomozygous115865637
7124360268124360269GA32GENIChomozygous116226636
7124360930124360931GA15GENIChomozygous116226637
7124364056124364057CT31GENIChomozygous116226638
7124364485124364486GA13GENIChomozygous115865651
7124364758124364759CT19GENIChomozygous116226639
7124365980124365981CT29GENIChomozygous116226640
7124366145124366146TC32GENIChomozygous115865653
7124366572124366573GA26GENIChomozygous116226641