chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1207136721207136722GT14GENIChomozygous61921617
1207136949207136950CCGG16GENIChomozygous61068686
1207137152207137153GA13GENIChomozygous61921618
1207137720207137727TATGTAG-------14GENIChomozygous61921619
1207138539207138540CCATAT14GENIChomozygous61921620
1207138629207138630CT19GENIChomozygous61068689
1207139873207139874TC13GENIChomozygous61068691
1207143663207143664AG13GENIChomozygous61921623
1207143740207143741CA23GENIChomozygous61921624
1207143760207143761AC19GENIChomozygous61921625
1207145024207145025TC6GENICheterozygous62804163
1207147413207147414TC12GENIChomozygous61921626
1207147684207147685A-10GENIChomozygous61068698
1207148204207148208TTTG----21GENIChomozygous61068699
1207149420207149421TA12GENIChomozygous61068700
1207149421207149422TA12GENIChomozygous61964028
1207150305207150306AG15GENIChomozygous61068708
1207150796207150797AG17GENIChomozygous61068709
1207150810207150811AAGGCCTT15GENIChomozygous61068710
1207150824207150825AG15GENIChomozygous61068711
1207151271207151272CA11GENIChomozygous61068712
1207151404207151405TG25GENIChomozygous61921627
1207151420207151421GA21GENIChomozygous61921628
1207151602207151603A-13GENIChomozygous61068713
1207152829207152830GA18GENIChomozygous61068714
1207153183207153184C-7GENIChomozygous62193293
1207153228207153229TC10GENIChomozygous61068715
1207155232207155233TC18GENIChomozygous61068717
1207157282207157283CCT10GENIChomozygous61068720
1207158393207158394T-19GENIChomozygous61068722
1207159465207159466TC16GENIChomozygous61068726
1207159986207159987AG18GENIChomozygous61068727
1207160017207160018AG15GENIChomozygous61921629
1207160067207160068TG17GENIChomozygous61921630
1207160366207160367AG14GENIChomozygous61068728
1207163015207163016TC22GENIChomozygous61068732