chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154876847748768478AAGGCCT28GENIChomozygous48304321
154876857948768580AG35GENIChomozygous48304322
154876858448768585CA34GENIChomozygous48304323
154876874748768748TC40GENIChomozygous48304324
154876875148768752AG42GENIChomozygous48304325
154876875748768758CA46GENIChomozygous48304326
154876877348768774GT48GENIChomozygous48304327
154876885548768856AG40GENIChomozygous48304328
154876918448769185CT37GENIChomozygous48304329
154876935248769353AG46GENIChomozygous48304330
154876938448769385AG54GENIChomozygous48304331
154876991848769919GA31GENIChomozygous48304332
154877141748771418AG19GENIChomozygous48304333
154877153648771537AG7GENIChomozygous48304334
154877187248771873CT23GENIChomozygous48304335
154877274948772750GC26GENIChomozygous48304336
154877289548772896CT29GENIChomozygous48304337
154877343748773438TA34GENICheterozygous48304340
154877560248775603TC39GENIChomozygous48304341
154877589348775894GA32GENIChomozygous48304342
154877738848777389TTA12GENIChomozygous48304343
154877857748778583CACACA------3GENIChomozygous48304344
154878052748780528CT20GENICpossibly homozygous48304345
154878052948780530TTCACCCTGGC19GENICpossibly homozygous48304346
154878108248781083TC25GENIChomozygous48304347
154878253748782538AG22GENIChomozygous48304348
154878263148782632TC27GENICheterozygous48304349
154878265148782652TC21GENICpossibly homozygous48304350
154878327048783271AC19GENIChomozygous48304351
154878328448783285GA20GENIChomozygous48304352
154878409148784092GA25GENIChomozygous48304353
154878417648784177TG23GENIChomozygous48304354
154878471548784716AC34GENIChomozygous48304355
154878514448785145AG34GENIChomozygous48304356