chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175398329053983291CT13GENIChomozygous884788263
175398448153984482TC18GENIChomozygous884788264
175398519453985195AC17GENIChomozygous884788265
175398725053987251AG19GENIChomozygous884788266
175398810953988110CT13GENICheterozygous884788267
175399312053993121AC14GENIChomozygous884788268
175399347153993472GC7GENIChomozygous884788269
175399390753993908GA30GENIChomozygous884788270
175399448553994486GA13GENIChomozygous884788271
175399836253998363AT22GENIChomozygous884788272
175400060254000603AT20GENIChomozygous884788273
175400275054002751CG5GENIChomozygous884788274
175400357954003580CA9GENIChomozygous884788275
175400402954004030GT29GENIChomozygous884788276
175400437254004373AG19GENIChomozygous884788277
175400458654004587CA13GENIChomozygous884788278
175400976554009766GA12GENIChomozygous884788279
175401080154010802AG32GENIChomozygous884788280
175401097654010977CT22GENIChomozygous884788281
175401238554012386TC14GENIChomozygous884788282
175401650154016502GC6GENICheterozygous884788283
175401771154017712CT16GENIChomozygous884788284
175401795154017952TC20GENIChomozygous884788285
175401848354018484CT16GENIChomozygous884788286
175402255854022559AG21GENIChomozygous884788287
175402314954023150CT13GENIChomozygous884788288
175402457954024580CT11GENIChomozygous884788289
175402475754024758AG14GENIChomozygous884788290