chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112418172624181727GA27GENIChomozygous998008532
112418279024182791GA26GENIChomozygous998008533
112418400424184005GT22GENIChomozygous998008534
112418400724184008TG22GENIChomozygous998008535
112418445924184460CA30GENIChomozygous998008536
112418490724184908AG16GENIChomozygous998008537
112418531824185319CA15GENIChomozygous998008538
112418567024185671TC20GENIChomozygous998008539
112418668324186684AT27GENIChomozygous998008540
112418684124186842GA32GENIChomozygous998008541
112418693024186931CT26GENIChomozygous998008542
112418718524187186AC28GENIChomozygous998008543
112418761624187617CT31GENIChomozygous998008544
112418796924187970CT24GENIChomozygous998008545
112418816124188162GA31GENIChomozygous998008546
112418862824188629AC19GENIChomozygous998008547
112418968824189689TC19GENIChomozygous998008548
112419055224190553CT30GENIChomozygous998008549
112419055524190556GA30GENIChomozygous998008550
112419071024190711AT28GENIChomozygous998008551
112419206224192063CG24GENIChomozygous998008552
112419265424192655CT21GENIChomozygous998008553
112419282224192823CT8GENIChomozygous998008554