chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124338558124338559CT24GENIChomozygous115865587
7124339161124339162GC26GENIChomozygous115865589
7124339853124339854CT29GENIChomozygous115865591
7124340923124340924GA10GENIChomozygous118286503
7124342549124342550CT28GENIChomozygous115865593
7124343113124343114GA11GENIChomozygous115865595
7124343393124343394CT27GENIChomozygous115865597
7124343396124343397TG26GENIChomozygous115865599
7124343439124343440CT32GENIChomozygous115865601
7124343520124343521TC30GENIChomozygous115865603
7124344290124344291CA19GENIChomozygous115865605
7124344357124344358TC20GENIChomozygous115865607
7124344511124344512GA30GENIChomozygous115865609
7124345384124345385GA36GENIChomozygous115865611
7124345385124345386GT36GENIChomozygous115865613
7124346017124346018AG20GENIChomozygous115865615
7124346977124346978TC17GENIChomozygous115865617
7124347456124347457CT25GENIChomozygous115865619
7124349089124349090TG28GENIChomozygous115865623
7124351265124351266AG28GENIChomozygous115865627
7124354044124354045TC35GENIChomozygous115865631
7124354543124354544TC22GENIChomozygous115865633
7124357262124357263CT18GENIChomozygous115865635
7124357590124357591CT39GENIChomozygous115865637
7124357877124357878CT20GENIChomozygous115865639
7124358197124358198CT22GENIChomozygous115865641
7124359642124359643CT24GENIChomozygous115865643
7124360478124360479GA24GENIChomozygous115865645
7124362635124362636CT23GENIChomozygous115865647
7124363343124363344GT29GENIChomozygous115865649
7124364485124364486GA22GENIChomozygous115865651
7124366145124366146TC16GENIChomozygous115865653
7124366324124366325CT23GENIChomozygous115865655
7124367436124367437CA31GENIChomozygous115865657
7124351259124351260TG27GENIChomozygous118259334
7124351260124351261GC27GENIChomozygous118259336