chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47849803478498035GA53GENIChomozygous112738433
47849902578499026TC46GENIChomozygous112738435
47849943178499432GA43GENIChomozygous112738437
47849967778499678AC40GENIChomozygous112738439
47850030178500302CT34GENIChomozygous119278356
47850051278500513GA54GENIChomozygous112738441
47850106578501066TA32GENIChomozygous112738443
47850111478501114G23GENIChomozygous128052217
47850030178500301AA35GENIChomozygous128052214
47850037578500376A23GENICheterozygous128052215
47850038278500384AG24GENICheterozygous128052216
47850112678501127A23GENIChomozygous128052218
47850148478501485GA55GENIChomozygous112738445
47850156478501565GC47GENIChomozygous112738447
47850168578501686G15GENIChomozygous128052219
47850170178501701A2GENIChomozygous128052220
47850201378502014CT42GENIChomozygous112738449
47850220178502202AG43GENICpossibly homozygous112738451
47850224978502250TC46GENIChomozygous112738453
47850237378502374TC46GENIChomozygous112738455
47850245678502457TC61GENIChomozygous112738457
47850262278502623TC46GENIChomozygous112738459
47850290978502910AG59GENIChomozygous112738462
47850342278503423CT51GENIChomozygous112738464
47850379878503799AG53GENIChomozygous112738466
47850456078504561AG66GENIChomozygous112738468
47850493478504935GA31GENIChomozygous112738470
47850529378505294GA48GENIChomozygous112738472
47850536478505365CT47GENIChomozygous112738474
47850755678507557GT41GENIChomozygous112738476
47850871978508720A71GENIChomozygous128052221
47850907578509076CA42GENICpossibly homozygous112738478
47851069378510694GA50GENIChomozygous112738486
47850927978509280GC59GENIChomozygous112738480
47850994978509950GT49GENIChomozygous112738482
47851055778510558GA48GENIChomozygous112738484
47851234778512348TG51GENIChomozygous112738488
47851323678513237GA56GENIChomozygous112738490
47851345678513457AC50GENIChomozygous112738492
47851382778513828GT55GENICpossibly homozygous112738494
47851428178514282TC52GENIChomozygous112738496
47851469378514694AG62GENIChomozygous112738498