chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101476216101476217CA17GENIChomozygous66168221
13101476217101476218CG17GENIChomozygous66168224
13101476218101476219CG16GENIChomozygous66168227
13101476219101476220CG16GENIChomozygous66168230
13101476220101476221CT16GENIChomozygous66168233
13101488049101488050CT59GENICheterozygous66168245
13101488088101488089CT27GENIChomozygous66168248
13101488097101488098CT25GENIChomozygous66168251
13101488151101488152CT15GENIChomozygous66168253
13101488172101488173AT20GENIChomozygous66168256
13101488184101488185CT22GENIChomozygous66168259