chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22506964825069649AG55GENIChomozygous109649208
22506990025069901TC50GENIChomozygous109649210
22506999025069991CT25GENIChomozygous109649212
22507061525070616CT55GENIChomozygous109649214
22507080825070809CT52GENIChomozygous109649215
22507197325071974CT54GENIChomozygous109649217
22507201925072020AG46GENIChomozygous109649219
22507254525072546AG41GENIChomozygous109649221
22507265425072655GA34GENIChomozygous109649223
22507408125074082AC44GENIChomozygous109649225
22507448025074481GA23GENIChomozygous109649227
22507502725075028GA35GENIChomozygous109649229
22507690125076902GC31GENIChomozygous109649233
22507711225077113AG49GENIChomozygous109649235
22507825825078259TC57GENIChomozygous109649237
22507884925078850TC39GENIChomozygous109649239
22508158825081589TC56GENIChomozygous109649245
22508168925081690AT40GENIChomozygous109649247
22508211225082113TC36GENIChomozygous109649249
22508246325082464GC48GENIChomozygous109649251
22508381625083817CT40GENICpossibly homozygous109649253
22508392125083922AC23GENIChomozygous110490996
22508516125085162CT34GENIChomozygous109649255
22508516225085163AG34GENIChomozygous109649257
22508596225085963TA32GENIChomozygous109649261
22508614725086148CT36GENIChomozygous109649263
22508703125087032GA32GENIChomozygous109649271
22508733825087339GA40GENICpossibly homozygous109649273
22508739825087399GC28GENIChomozygous110675544
22508787625087877CT22GENIChomozygous109649275
22508814725088148GA33GENIChomozygous109649277
22509227025092271TC27GENIChomozygous109649329
22509506725095068TC29GENIChomozygous111323033
22507402325074024GT31GENICheterozygous120122361
22508392025083921CA23GENIChomozygous120122363
22508739525087396CA30GENIChomozygous120122365
22509506825095069CG28GENIChomozygous120122367