chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121597633515976336CT18GENICheterozygous935995257
121597720915977210GA23GENIChomozygous935995258
121597730215977303GA16GENIChomozygous935995259
121598192515981926CA21GENIChomozygous935995260
121599406215994063CT16GENIChomozygous935995261
121599423415994235GA18GENIChomozygous935995262
121599431515994316AG14GENIChomozygous935995263
121599500615995007GT24GENIChomozygous935995264
121599507315995074AG12GENIChomozygous935995265
121599589115995892GT10GENIChomozygous935995266
121599716615997167CT20GENIChomozygous935995267
121599722615997227AG18GENIChomozygous935995268
121599734215997343TC12GENIChomozygous935995269
121599970915999710CT27GENIChomozygous935995270
121599975915999760CT15GENIChomozygous935995271
121600053416000535TC16GENIChomozygous935995272
121600117316001174TC10GENIChomozygous935995273
121600203316002034AG19GENIChomozygous935995274
121600238116002382GA13GENIChomozygous935995275
121600568316005684CT6GENIChomozygous935995276
121600590716005908TC18GENIChomozygous935995277
121600768616007687AC20GENIChomozygous935995278
121600879516008796AG14GENIChomozygous935995279
121600901716009018TC12GENIChomozygous935995280
121600924616009247AG11GENIChomozygous935995281
121600963716009638CT10GENIChomozygous935995282
121601035116010352AC24GENIChomozygous935995283
121601044516010446CT13GENIChomozygous935995284
121601053216010533CT11GENIChomozygous935995285
121601066516010666TC28GENIChomozygous935995286
121601117816011179GA8GENIChomozygous935995287