chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117215131117215132AG69GENIChomozygous112818305
4117216867117216868GA54GENIChomozygous112818307
4117217237117217238CT63GENIChomozygous119407029
4117217832117217833TC56GENIChomozygous112818311
4117219725117219726TG49GENIChomozygous112818315
4117220604117220605TC50GENIChomozygous113048274
4117221254117221255TC43GENIChomozygous112818317
4117222794117222795AG46GENIChomozygous112818319
4117225034117225035CT58GENIChomozygous119407030
4117225168117225169CT49GENIChomozygous119407031
4117226125117226126GT48GENICpossibly homozygous119527415
4117226184117226185AG50GENIChomozygous112818321
4117228158117228159GA56GENIChomozygous112818327
4117228447117228448T47GENIChomozygous128072512