chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116724245067242451TG25GENIChomozygous50807788
116724312667243127GA22GENIChomozygous51117940
116724478267244783GGT39GENIChomozygous50807789
116724499667244999AAT---5GENIChomozygous50807790
116724520467245212TCTCTCTC--------9GENICheterozygous50807792
116724520667245212TCTCTC------9GENICpossibly homozygous50883230
116724537067245371CT21GENIChomozygous50883232
116724537167245372CCTCACACTT19GENIChomozygous50807793
116724539467245395CT25GENIChomozygous50807795
116724544067245441CA27GENIChomozygous50807797
116724570867245714AAAAAG------7GENIChomozygous50807800
116724588967245890AT26GENIChomozygous50807802
116724655767246558TC30GENIChomozygous50807803
116724688167246882TTGG7GENIChomozygous50807805
116724688367246884TTGG8GENIChomozygous50807807
116724688567246886TTGG9GENIChomozygous50807812
116724701467247015AG23GENIChomozygous50807813
116724702067247021CT24GENIChomozygous50807815
116724703367247034TC24GENIChomozygous50807816
116724712367247124TC22GENIChomozygous50807818
116724722267247223A-29GENIChomozygous50807819
116724723267247233CG32GENIChomozygous50807821
116724734967247350TG25GENIChomozygous50807822
116724768967247691GT--23GENIChomozygous50807823