chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101476216101476217CA13GENIChomozygous66168221
13101476217101476218CG13GENIChomozygous66168224
13101476218101476219CG12GENIChomozygous66168227
13101476219101476220CG12GENIChomozygous66168230
13101476220101476221CT11GENIChomozygous66168233
13101488049101488050CT78GENICheterozygous66168245
13101488088101488089CT34GENICheterozygous66168248
13101488097101488098CT29GENIChomozygous66168251
13101488151101488152CT14GENIChomozygous66168253
13101488172101488173AT17GENIChomozygous66168256
13101488184101488185CT21GENIChomozygous66168259