chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76296374962963750CT21INTERGENIChomozygous68849134
76297193162971932AT51INTERGENIChomozygous68849136
76297555362975554GT12INTERGENIChomozygous68849138
76298060262980603TC27INTERGENICheterozygous68849140
76298061462980615TC26INTERGENICheterozygous68849142
76298070162980702TA39INTERGENICheterozygous68849144
76298091062980911CT39INTERGENICheterozygous68849146
76298449162984492AG15INTERGENICheterozygous68849152
76298454062984541CT17INTERGENICheterozygous68849154
76298455162984552GA14INTERGENICheterozygous68849156
76298462362984624GA12INTERGENICheterozygous68849158
76299342862993429CT30INTERGENICpossibly homozygous68849168
76299413162994132AT44INTERGENIChomozygous68849170
76299421062994211AC36INTERGENIChomozygous68849172
76299469562994696CA18INTERGENIChomozygous68849174
76300130263001303TC37INTERGENIChomozygous68849176
76301128563011286AT23INTERGENICheterozygous69442307
76301128963011290AT22INTERGENICheterozygous69442309
76301297663012977TC49INTERGENIChomozygous68849178
76302142463021425AG17INTERGENICheterozygous68849180
76302480363024804GA56INTERGENICpossibly homozygous68849182