chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2046980014698002GA14GENIChomozygous63570049
2046993544699355GA28GENIChomozygous63570053
2046994174699418TG22GENIChomozygous63570055
2046994554699456TC18GENIChomozygous63570057
2046996044699605AC5GENIChomozygous63570067
2047001724700173TC31GENIChomozygous63338081
2047002774700278CT29GENICpossibly homozygous63338086
2047003874700388AG13GENIChomozygous63338091
2047004164700417AT7GENIChomozygous63338093
2047005334700534AG30GENIChomozygous63570073
2047005854700586GA24GENIChomozygous63570075
2047006294700630AT4GENIChomozygous63570081
2047006614700662AG21GENIChomozygous63570083
2047007804700781CT16GENIChomozygous63338104
2047008564700857AT14GENIChomozygous63570089
2047009414700942AG20GENIChomozygous63570091
2047013454701346GT7GENIChomozygous63570117
2047013494701350TA9GENIChomozygous63338125
2047013934701394CT26GENIChomozygous63740293
2047013944701395TC28GENIChomozygous63740294
2047015614701562CT18GENIChomozygous63338127
2047015744701575GA15GENIChomozygous63570119
2047016824701683TC14GENIChomozygous63338133
2047016884701689TC15GENIChomozygous63338134
2047017244701725CG16GENIChomozygous63570121
2047018124701813AG20GENIChomozygous63338139
2047018134701814TG20GENIChomozygous63570123
2047018654701866GA18GENIChomozygous63338142
2047019634701964CG14GENIChomozygous63570125
2047019894701990TC19GENIChomozygous63338148
2047020044702005AG20GENIChomozygous63570127
2047021144702115GA10GENIChomozygous63570129
2047021194702120GA10GENIChomozygous63338150
2047021544702155CA4GENIChomozygous63338152
2047022534702254TC26GENIChomozygous63338159
2047023054702306TC20GENIChomozygous63338160
2047023294702330TA15GENIChomozygous63570137
2047023404702341CG8GENIChomozygous63338161
2047023584702359GC18GENIChomozygous63338162
2047024214702422GC5GENIChomozygous63570139
2047024644702465TC5GENIChomozygous63338171
2047024694702470TC16GENIChomozygous63570143
2047025304702531AG14GENIChomozygous63570145