chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4186788077186788078CCGT12GENICheterozygous58674142
4186788077186788078CCGTGT12GENICheterozygous59157975
4186796313186796314TC18GENIChomozygous58516337
4186800237186800238GA23GENIChomozygous58516345
4186800253186800254AC22GENIChomozygous58516347
4186800577186800578TC26GENIChomozygous58516349
4186800808186800809AG21GENIChomozygous58516351
4186801043186801044CG21GENIChomozygous58516353
4186801355186801356AG17GENIChomozygous58516355
4186801394186801395AG18GENIChomozygous58516357
4186801444186801445A-18GENIChomozygous58516359
4186801930186801931TTTGCTCTCCCAAATC24GENIChomozygous58516361
4186802271186802272AT33GENIChomozygous58516363
4186802639186802640TC16GENIChomozygous58516365
4186802735186802736TC24GENIChomozygous58516367
4186803270186803271CT24GENIChomozygous58516369
4186806497186806499TG--10GENIChomozygous58360652
4186801330186801331GA18GENIChomozygous59658743
4186807535186807536CT18GENIChomozygous59658744
4186810735186810736AC3GENIChomozygous58360654
4186810738186810739AT5GENIChomozygous58298656
4186810803186810804CCTCT8GENICheterozygous58408944
4186810704186810705TTTCC3GENIChomozygous58704125