chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47849617178496172AG34GENIChomozygous119517325
47849618978496189AGG33GENIChomozygous131354250
47849627778496278AG39GENIChomozygous119517327
47849765878497659CT53GENIChomozygous119517329
47849929578499295T4GENICheterozygous131354251
47850030178500302CT46GENIChomozygous119278356
47850106578501066TA25GENIChomozygous112738443
47849803478498035GA51GENIChomozygous112738433
47849902578499026TC35GENIChomozygous112738435
47849943178499432GA31GENIChomozygous112738437
47849967778499678AC44GENIChomozygous112738439
47849931178499312GA6GENICheterozygous131370167
47850030178500301AA44GENIChomozygous128052214
47850038278500384AG40GENIChomozygous128052216
47850111478501114G20GENIChomozygous128052217
47850112678501127A17GENIChomozygous128052218
47850148478501485GA37GENIChomozygous112738445
47850156478501565GC37GENIChomozygous112738447
47850168578501686G11GENIChomozygous128052219
47850172978501747AGAGAGAGAGAGAGAGGA9GENIChomozygous134933009
47850220178502202AG38GENIChomozygous112738451
47850224978502250TC52GENIChomozygous112738453
47850237378502374TC42GENIChomozygous112738455
47850290978502910AG36GENIChomozygous112738462
47850379878503799AG46GENIChomozygous112738466
47850420778504208TA53GENIChomozygous113125653
47850475378504754CA43GENIChomozygous119517333
47850734078507341TG49GENIChomozygous113352366
47850741178507412TC50GENIChomozygous119517335
47850755678507557GT46GENIChomozygous112738476
47850825778508257T47GENICpossibly homozygous131354252
47850927978509280GC34GENIChomozygous112738480
47851234778512348TG45GENIChomozygous112738488
47851345678513457AC44GENIChomozygous112738492
47851399978514000T47GENIChomozygous131354253
47851428178514282TC50GENIChomozygous112738496
47850169878501700GG6GENIChomozygous129902753
47850903378509034TC56GENIChomozygous113459011