chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266483552266483553CT19GENIChomozygous108638216
1266485652266485653TA29GENIChomozygous108638217
1266486751266486752GA10GENIChomozygous108638219
1266486995266486996CT25GENIChomozygous108638220
1266487314266487315AG4GENICheterozygous125411091
1266487893266487894CT14GENIChomozygous108638221
1266488317266488318AG16GENIChomozygous108638222
1266488453266488454TG7GENIChomozygous108638223
1266488457266488458CG8GENIChomozygous108638224
1266488584266488585TC10GENIChomozygous108638225
1266491321266491322CT19GENIChomozygous108638227
1266491378266491379GA19GENIChomozygous108638228
1266491881266491882GA17GENIChomozygous108638229
1266492131266492132TA23GENIChomozygous108638230
1266492999266493000GA11GENIChomozygous108638235
1266493001266493002GT12GENIChomozygous108638236
1266493020266493021CT12GENIChomozygous108638237
1266493113266493114CT12GENIChomozygous108638238
1266493239266493240GA15GENIChomozygous108638239
1266494063266494064GA21GENIChomozygous108638242
1266494693266494694AG13GENIChomozygous108638243
1266495790266495791GA16GENIChomozygous108638245
1266496035266496036GA14GENICheterozygous108638246
1266497641266497642TG27GENIChomozygous108638251
1266497715266497716AG14GENIChomozygous108638252
1266497812266497813CT22GENIChomozygous108638253
1266501507266501508GA8GENICheterozygous108638258
1266503241266503242AG5GENIChomozygous108638260
1266507858266507859TC18GENIChomozygous108638266
1266510619266510620TC22GENIChomozygous108638267