chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116724245067242451TG16GENIChomozygous50807788
116724312667243127GA17GENIChomozygous51117940
116724478267244783GGT9GENIChomozygous50807789
116724499667244999AAT---4GENIChomozygous50807790
116724520467245212TCTCTCTC--------4GENICheterozygous50807792
116724520667245212TCTCTC------4GENICheterozygous50883230
116724537067245371CT19GENIChomozygous50883232
116724537167245372CCTCACACTT19GENIChomozygous50807793
116724539467245395CT15GENIChomozygous50807795
116724544067245441CA14GENIChomozygous50807797
116724568467245685AC5GENIChomozygous50807798
116724568567245686GA4GENIChomozygous51187217
116724569067245691GGA6GENIChomozygous51187218
116724570867245714AAAAAG------8GENIChomozygous50807800
116724588967245890AT12GENIChomozygous50807802
116724655767246558TC8GENIChomozygous50807803
116724688367246884TTGG3GENIChomozygous50807807
116724701467247015AG19GENIChomozygous50807813
116724702067247021CT20GENIChomozygous50807815
116724703367247034TC18GENIChomozygous50807816
116724712367247124TC3GENIChomozygous50807818
116724722267247223A-9GENIChomozygous50807819
116724723267247233CG12GENIChomozygous50807821
116724734967247350TG19GENIChomozygous50807822
116724768967247691GT--6GENIChomozygous50807823