chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81128000511280006AC18GENIChomozygous142034254
81128185611281857TG13GENIChomozygous143385405
81128289211282893CT11GENIChomozygous143385406
81128432611284327AG11GENIChomozygous143385407
81128487511284876AG21GENIChomozygous142034257
81128544711285448AG19GENIChomozygous143385408
81128567611285677CT18GENIChomozygous142034258
81128740111287402GC17GENIChomozygous142034259
81128771711287718AG17GENIChomozygous142034260
81128776411287765CT17GENIChomozygous142034261
81128987211289873AG17GENIChomozygous142034264
81129062011290621AT12GENIChomozygous143385409
81129120111291202AG27GENIChomozygous142034265
81129226611292267GA20GENIChomozygous142034267
81129334711293348CT22GENICpossibly homozygous143385410
81129353211293533CT23GENIChomozygous142034268
81129493211294933A18GENIChomozygous142016921
81129543711295438GA19GENIChomozygous142034269
81130055011300551C12GENIChomozygous142016928
81130117111301175ATGT17GENIChomozygous142016929
81130145411301455T11GENIChomozygous142016930
81129520011295200A16GENIChomozygous143374561
81129716011297161CT26GENIChomozygous143385411
81130276011302761GA12GENIChomozygous143385412
81130443211304433AG7GENIChomozygous142034272