chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117215131117215132AG18GENIChomozygous112818305
4117216867117216868GA19GENIChomozygous112818307
4117217237117217238CT24GENIChomozygous119407029
4117217832117217833TC20GENIChomozygous112818311
4117219725117219726TG10GENIChomozygous112818315
4117220604117220605TC24GENIChomozygous113048274
4117221254117221255TC25GENIChomozygous112818317
4117222794117222795AG18GENIChomozygous112818319
4117225034117225035CT26GENIChomozygous119407030
4117225168117225169CT23GENIChomozygous119407031
4117226184117226185AG12GENIChomozygous112818321
4117228158117228159GA17GENIChomozygous112818327
4117226125117226126GT10GENIChomozygous119527415
4117228447117228448T23GENIChomozygous128072512