chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261193144261193145TC16GENIChomozygous120881302
1261193149261193150CA15GENIChomozygous120881303
1261193162261193163GT13GENIChomozygous120881304
1261193360261193361TC18GENIChomozygous108629170
1261196631261196632CG23GENIChomozygous108629174
1261198333261198334CT31GENIChomozygous120881305
1261198832261198833GA15GENIChomozygous120881306
1261201046261201047GA28GENIChomozygous108629178
1261203906261203907AC17GENIChomozygous108629185
1261204612261204613GA25GENIChomozygous120881307
1261205342261205343AG14GENIChomozygous108629186
1261206259261206260AC26GENIChomozygous120881308
1261206346261206347TC38GENIChomozygous108629188
1261207292261207293AT20GENIChomozygous120881309
1261207793261207794TG25GENIChomozygous108629189
1261209466261209467TG15GENIChomozygous120881310
1261209553261209554CG24GENIChomozygous120881311
1261210640261210641AG27GENIChomozygous120881312
1261210677261210678CG21GENIChomozygous120881313
1261215388261215389TC25GENICheterozygous120881314
1261220337261220338AG3GENIChomozygous120881315
1261220378261220379TC7GENIChomozygous120881316
1261220644261220645AC6GENIChomozygous120881317
1261220653261220654AC5GENIChomozygous120881318
1261221533261221534TA34GENIChomozygous120881319
1261221991261221992GA25GENIChomozygous120881320
1261222343261222344AC24GENICpossibly homozygous120881321
1261222612261222613TC32GENIChomozygous108629197
1261224893261224894GA14GENIChomozygous120881322
1261226822261226823CT31GENIChomozygous120881323
1261227832261227833GA35GENIChomozygous120881324
1261228613261228614CT11GENIChomozygous120881325