chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124339161124339162GC18GENIChomozygous115865589
7124339853124339854CT16GENIChomozygous115865591
7124340150124340151TC20GENIChomozygous116226616
7124340593124340594GT37GENIChomozygous116226617
7124341640124341641CT28GENIChomozygous116226618
7124342221124342222AG21GENIChomozygous116226619
7124342808124342809AG35GENIChomozygous116226620
7124343070124343071TC24GENIChomozygous116226621
7124344290124344291CA24GENIChomozygous115865605
7124344725124344726AG13GENIChomozygous116226622
7124346017124346018AG30GENIChomozygous115865615
7124346085124346086CT28GENIChomozygous116226624
7124346457124346458AC23GENIChomozygous116226625
7124346977124346978TC24GENIChomozygous115865617
7124347350124347351CT19GENIChomozygous116226626
7124349089124349090TG14GENIChomozygous115865623
7124350157124350158GA19GENIChomozygous116226628
7124350303124350304TC22GENIChomozygous116226629
7124350783124350784CT14GENIChomozygous116226630
7124351259124351260TG18GENIChomozygous118259334
7124351260124351261GC19GENIChomozygous118259336
7124351265124351266AG16GENIChomozygous115865627
7124354044124354045TC15GENIChomozygous115865631
7124354543124354544TC24GENIChomozygous115865633
7124355098124355099CT22GENIChomozygous116226631
7124355645124355646GA17GENIChomozygous116226632
7124356412124356413AG17GENIChomozygous116226633
7124357561124357562GC23GENIChomozygous116226635
7124357590124357591CT24GENIChomozygous115865637
7124360268124360269GA15GENIChomozygous116226636
7124360930124360931GA22GENIChomozygous116226637
7124364056124364057CT22GENIChomozygous116226638
7124364485124364486GA14GENIChomozygous115865651
7124364758124364759CT15GENIChomozygous116226639
7124365980124365981CT22GENIChomozygous116226640
7124366145124366146TC21GENIChomozygous115865653
7124366572124366573GA26GENIChomozygous116226641