chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2118720971118720972AG41GENIChomozygous109994269
2118720973118720974AG42GENIChomozygous109994271
2118721123118721124GA42GENIChomozygous109994273
2118722047118722048CT47GENIChomozygous109994275
2118722058118722059AG46GENIChomozygous109994277
2118722375118722376GA51GENIChomozygous109994279
2118724854118724855CT57GENIChomozygous109994281
2118725312118725312T50GENICpossibly homozygous127671050
2118727673118727674TC51GENIChomozygous109994282
2118730025118730026A57GENIChomozygous127671051
2118730090118730091GC47GENIChomozygous109994284
2118730948118730949GC39GENIChomozygous109994286
2118731241118731242AG46GENIChomozygous109994288
2118731268118731269GA49GENIChomozygous109994290
2118731445118731446T10GENICheterozygous127671052
2118732213118732214GA45GENIChomozygous109994292
2118732446118732447AT18GENIChomozygous109994294
2118733006118733007GA53GENIChomozygous109994296
2118733291118733292CA65GENIChomozygous109994297
2118733414118733415TC54GENIChomozygous109994299
2118733979118734120TTTTTTTTTTTTTTTTTTTTTTTTGAGTTTAAGCTCCTGTGGGAACTTAGAAGCTGGGTTCCGAGGATAGAAAACTGGCTTGTAAAGTTCAGGGGGAAGTTTGAGAGTCACAGTCTCTATGAGGATATTCATCTTTTTTTT23GENIChomozygous127671053
2118734296118734297CT50GENIChomozygous109994301
2118734738118734739CT51GENIChomozygous109994303
2118735068118735069CT53GENIChomozygous109994305
2118736363118736364AT61GENIChomozygous109994307
2118738957118738958AG54GENIChomozygous109994308
2118739762118739763TG65GENIChomozygous109994310
2118740367118740368GT57GENIChomozygous109994312
2118741199118741200AT71GENIChomozygous109994314
2118741313118741314GA60GENIChomozygous109994316
2118741530118741530A61GENIChomozygous127671054
2118742103118742104CT50GENIChomozygous109994317
2118742152118742153CA40GENIChomozygous109994319
2118742300118742301CT48GENIChomozygous109994321
2118742974118742975AG68GENIChomozygous109994323
2118743124118743124G26GENICheterozygous127671055
2118743547118743548AG42GENIChomozygous109994325
2118745105118745106AC60GENIChomozygous109994327