chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2225310908225310909CT42GENICpossibly homozygous110271255
2225314676225314677TG48GENIChomozygous110271257
2225314896225314897TC58GENIChomozygous110271259
2225315382225315383TC28GENIChomozygous110271261
2225315902225315903CT43GENIChomozygous110271263
2225315978225315979GA37GENIChomozygous110271265
2225316223225316224CT27GENIChomozygous110271267
2225316251225316252CT36GENIChomozygous110271269
2225316847225316848CT45GENIChomozygous110271271
2225316947225316948TC20GENIChomozygous110271273
2225317442225317443AT44GENIChomozygous110271275
2225317599225317600TC22GENIChomozygous110271277
2225317802225317803AG37GENIChomozygous110271278
2225319186225319187GT45GENIChomozygous110271280
2225319628225319629TC35GENIChomozygous110271282
2225320208225320209AG57GENIChomozygous110271284
2225320266225320267AG51GENIChomozygous110271286