chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230186991230186992TC8GENIChomozygous125607089
2230188282230188283GA15GENIChomozygous125607090
2230190132230190133GA11GENIChomozygous125607091
2230190164230190165CT11GENIChomozygous125607092
2230190400230190401TG6GENIChomozygous125672567
2230190743230190744AG18GENIChomozygous125607093
2230190938230190939GT5GENIChomozygous125607094
2230190940230190941CT3GENICheterozygous125703359
2230190941230190942AC4GENIChomozygous125607095
2230190943230190944AC10GENIChomozygous125607096
2230191387230191388GC14GENIChomozygous125607097
2230191917230191918GA29GENIChomozygous125607098
2230191997230191998GA20GENIChomozygous125607099
2230192253230192254AG16GENIChomozygous125607100
2230192383230192384TC4GENIChomozygous125607101
2230192388230192389AC5GENIChomozygous125607102
2230192576230192577GC20GENICpossibly homozygous125607103
2230192901230192902TC33GENIChomozygous125607104
2230193202230193203TC14GENIChomozygous125607105
2230193737230193738TA12GENIChomozygous125672569
2230193980230193981CT26GENIChomozygous125607106
2230194167230194168GA25GENIChomozygous125607107
2230194437230194438CT23GENIChomozygous125607108
2230194462230194463TA26GENIChomozygous125607109
2230195351230195352CT12GENIChomozygous125607110
2230195409230195410CA31GENIChomozygous125607111
2230195590230195591GT8GENIChomozygous125607112
2230195703230195704CT8GENIChomozygous125607113
2230195777230195778CT11GENIChomozygous125607114
2230195833230195834GA25GENIChomozygous125607115
2230195972230195973GA23GENIChomozygous125607116
2230196317230196318TC17GENIChomozygous125607117
2230196424230196425TG26GENIChomozygous125607118
2230196611230196612GA19GENIChomozygous125607119
2230197863230197864TC15GENIChomozygous125607120
2230198100230198101CT7GENIChomozygous125607121
2230198250230198251TA29GENIChomozygous125607122