chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117215131117215132AG71GENIChomozygous112818305
4117216867117216868GA56GENIChomozygous112818307
4117217237117217238CT67GENIChomozygous119407029
4117217832117217833TC50GENIChomozygous112818311
4117219725117219726TG42GENIChomozygous112818315
4117221254117221255TC49GENIChomozygous112818317
4117222794117222795AG51GENIChomozygous112818319
4117225034117225035CT58GENIChomozygous119407030
4117225168117225169CT44GENICpossibly homozygous119407031
4117220604117220605TC39GENIChomozygous113048274
4117226184117226185AG50GENIChomozygous112818321
4117228158117228159GA61GENIChomozygous112818327
4117228447117228448T45GENIChomozygous128072512
4117226125117226126GT47GENIChomozygous119527415