chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2220647919220647920TC15GENICheterozygous530011669
2220656203220656204GA24GENIChomozygous530011670
2220657570220657571A-14GENICheterozygous693663226
2220659116220659120GTGT----6GENICheterozygous693663228
2220661462220661463AAAGAG7GENICpossibly homozygous693663229
2220662194220662196TG--2GENIChomozygous693663231
2220665461220665462AAATAC14GENIChomozygous693663233
2220665503220665504TTAC24GENICheterozygous693663234
2220669390220669391CG13GENIChomozygous531581569
2220671977220671978CCA17GENICheterozygous693663236
2220682962220682963AG23GENIChomozygous530011671
2220685840220685841GC13GENIChomozygous531581570
2220695081220695082GGGT9GENICheterozygous693663237
2220695081220695082GGGTGT9GENICheterozygous693663238
2220696546220696547AT26GENIChomozygous531581571
2220696548220696549GT26GENIChomozygous531581572
2220698791220698792TG14GENICpossibly homozygous531581573
2220700058220700059CCT9GENICheterozygous693663239
2220700430220700431A-12GENIChomozygous693663241
2220700435220700436TTA12GENIChomozygous693663242
2220700517220700521TTTT----3GENIChomozygous693663243
2220710766220710767TG26GENIChomozygous530011672
2220714534220714535C-3GENIChomozygous693663246
2220714534220714535CCA25GENIChomozygous693663247
2220721362220721363TTAC5GENICheterozygous693663249