chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3152929849152929850AG22GENIChomozygous136842018
3152929884152929885GA16GENIChomozygous136842019
3152929897152929898AG17GENIChomozygous136842020
3152930226152930227T13GENIChomozygous136596266
3152930232152930233GT12GENIChomozygous136842021
3152930311152930312T11GENIChomozygous136596267
3152930361152930362TG15GENIChomozygous136842022
3152930577152930578AG11GENIChomozygous136842023
3152930638152930639CT11GENIChomozygous136842024
3152930737152930738AG15GENIChomozygous136842025
3152930796152930797AG19GENIChomozygous136842026
3152931129152931130CT14GENIChomozygous136842027
3152931168152931169GA20GENIChomozygous136842028
3152932409152932410AG21GENIChomozygous136842029
3152932429152932430CT21GENIChomozygous136842030
3152933541152933542TG20GENIChomozygous136842031
3152933976152933977CG19GENIChomozygous136842032
3152934230152934231TC27GENIChomozygous136842033
3152934862152934863TC20GENIChomozygous136842037
3152932141152932142GC20GENIChomozygous154148258
3152932151152932152TG25GENIChomozygous154148259
3152934617152934618GA18GENIChomozygous136842034
3152934796152934797GC26GENIChomozygous136842035
3152934797152934798CA26GENIChomozygous136842036
3152935837152935838CT23GENIChomozygous136842038
3152936234152936235CT22GENIChomozygous136842039