chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142277534142277535AG27GENIChomozygous55757060
5142277832142277833T-9GENIChomozygous55757061
5142277910142277911AAC1GENIChomozygous55757062
5142278064142278065A-3GENIChomozygous55757063
5142278702142278703CT47GENIChomozygous55757064
5142278801142278802CT63GENIChomozygous55757065
5142278900142278901TG54GENICheterozygous55757066
5142279015142279016AG77GENICpossibly homozygous55757067
5142279447142279448CT29GENIChomozygous55757068
5142279586142279587GA21GENIChomozygous55757069