chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75846351458463516TC--23GENIChomozygous53930141
75847101758471020CAA---27GENICheterozygous53930143
75847450558474508CCC---24GENICheterozygous53930145
75847450758474508C-24GENICpossibly homozygous53930147
75848871558488716A-20GENICheterozygous53930149
75848993158489932C-14GENICheterozygous53930151
75851524958515250AG82GENICheterozygous53930153
75851535558515356AG160GENICheterozygous53930155
75851727958517280AC31GENICheterozygous53930157
75852836458528368GTGT----16GENICheterozygous53930159
75852866358528664CT35GENIChomozygous53930161
75852917958529183ACAC----24GENICheterozygous53930163
75852923058529231TA42GENIChomozygous53930164
75853438658534387CT18GENICheterozygous53930166
75854390358543904GC26GENIChomozygous53930168
75854405758544058C-17GENIChomozygous53930170
75854513158545132GGT7GENIChomozygous53930172
75855640358556404AAG4GENIChomozygous53930173
75856242558562426TTAC28GENIChomozygous53930175
75856251958562521AC--12GENICheterozygous53930177
75857059458570595AAT28GENIChomozygous53930179
75857093358570934G-50GENIChomozygous53930181
75857269058572691GT44GENICheterozygous53930183
75858849258588493T-9GENIChomozygous53930185
75858853858588539TTA16GENIChomozygous53930187
75858873958588740G-34GENIChomozygous53930189
75858888458588885AATG23GENIChomozygous53930190
75859240458592405A-18GENICheterozygous53930192
75859556358595564CA12GENICheterozygous53930194