chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117215131117215132AG9GENIChomozygous112818305
4117216867117216868GA10GENIChomozygous112818307
4117217476117217477CT27GENIChomozygous112818309
4117217832117217833TC21GENIChomozygous112818311
4117221254117221255TC23GENIChomozygous112818317
4117222794117222795AG19GENIChomozygous112818319
4117225598117225599AT8GENIChomozygous119313202
4117225599117225600TC8GENIChomozygous119313204
4117225602117225603AC6GENIChomozygous119313206
4117225605117225606AT2GENIChomozygous119313208
4117226184117226185AG9GENIChomozygous112818321
4117227533117227534TC15GENIChomozygous112818323
4117228158117228159GA17GENIChomozygous112818327