chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
54933723649337237TC20GENIChomozygous141722925
54933742749337428CT21GENIChomozygous141722927
54933768349337684GT19GENIChomozygous146129644
54933820849338209CT19GENIChomozygous141722928
54933855549338555TTTG25GENICpossibly homozygous141681593
54933860349338604GA28GENICpossibly homozygous146129645
54933864349338644CT30GENIChomozygous137459165
54933896449338965GT27GENIChomozygous137459166
54933908249339083GA26GENICpossibly homozygous137459168
54933962949339630TG14GENIChomozygous141722929
54933972149339722GA19GENIChomozygous146129646
54933991549339916AC20GENIChomozygous146129647
54934068249340683TC12GENIChomozygous137459171
54934137049341371TC29GENIChomozygous141722930
54934143249341433CA23GENIChomozygous141722931
54934219949342200AC12GENICheterozygous403892351
54934220049342201AC12GENICheterozygous154287884
54933922249339223AT18GENICheterozygous403892349
54934219949342200A12GENICheterozygous403892350
54934077649340777CT15GENIChomozygous154287882
54934220049342201A12GENICheterozygous403892352
54934220149342202A12GENICheterozygous403892353
54934220149342202AC12GENICheterozygous403892354
54934256549342566AG20GENIChomozygous137459173
54934327349343274GC25GENIChomozygous137459175
54934330449343305TC18GENIChomozygous137459176
54934337349343374TG18GENIChomozygous137459177
54934348249343483GA12GENIChomozygous146129648
54934358049343581TC13GENIChomozygous137459178
54934376249343763CA11GENIChomozygous137459181
54934418449344185C22GENIChomozygous137306809
54934399449343994G17GENIChomozygous137306808
54934478349344784AT25GENIChomozygous137459183
54934481549344816TC18GENIChomozygous137459184
54934486549344866CT16GENIChomozygous141722933
54934494849344949TG7GENICheterozygous154287885
54934494849344949T7GENIChomozygous403892355
54934560349345604AT19GENIChomozygous146129649