chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121791381717913818C12GENIChomozygous128967096
121791654017916540A13GENIChomozygous128967097
121791654417916545TC12GENIChomozygous115275304
121791661617916617CG17GENIChomozygous115275306
121791661717916618CG17GENIChomozygous115275308
121791661817916619AT17GENIChomozygous115275310
121791662717916628TG19GENIChomozygous115275312
121791664217916643A19GENIChomozygous128967098
121791664817916649TG19GENIChomozygous115275316
121791967417919675CT7GENIChomozygous115275328
121791967617919677CT6GENIChomozygous115275330
121791967817919679CA6GENIChomozygous115275332
121791968217919683GC6GENIChomozygous115275334
121791968817919689TA6GENIChomozygous115275336
121791968917919690GA6GENIChomozygous115275338
121791969217919693CT5GENIChomozygous115275340
121791969817919699TC3GENIChomozygous115421509
121791652517916526CG11GENIChomozygous115365341
121791969617919697TC4GENIChomozygous115421507
121791970117919702GA3GENIChomozygous115421511
121791970417919705AC2GENIChomozygous115275342
121791970917919710GA2GENIChomozygous115275344
121791971917919720TA2GENIChomozygous123601990
121792054417920546AC11GENICheterozygous133428534
121793674017936740AGGGGGC3GENIChomozygous128967115
121793674817936748C3GENIChomozygous128967116
121793675417936754AGCA4GENIChomozygous128967117
121793676017936760A6GENIChomozygous128967118
121793676417936765G8GENIChomozygous128967119
121795655617956556A15GENIChomozygous128967133
121795662817956629GA15GENIChomozygous115275498
121795671217956713C15GENIChomozygous128967134
121795672417956724T15GENIChomozygous128967135
121795673117956732C16GENIChomozygous128967136
121795675217956752C14GENIChomozygous128967137
121795676117956761CCTCCTCTTTCCCCCTCCCTCCTTCTCTTCCTTCTTCCTTCTCCTCTCTCTTTCCCTTTTCTCCTCTTCCTCCTCTTCCTCCTCCTCCT12GENIChomozygous130406287
121795674217956743CT15GENIChomozygous115581059
121795669317956694AG18GENIChomozygous115505304
121795669417956695GA18GENIChomozygous115505306