chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47075584370755844CT43GENIChomozygous112702177
47075585370755854CA37GENIChomozygous112702179
47075587070755871AT34GENIChomozygous112702181
47075597770755978CT29GENIChomozygous112702183
47075603970756040CG35GENIChomozygous112702185
47075611370756114AG38GENIChomozygous112702187
47075613570756136GT39GENIChomozygous112702189
47075617570756176CT32GENIChomozygous112702191
47075642870756429GT28GENIChomozygous112702195
47075653470756535CA42GENIChomozygous112702197
47075671670756717AG38GENIChomozygous112702201
47075681770756818AT43GENIChomozygous112702203
47075682970756830TC42GENIChomozygous112702205
47075686270756863GA51GENIChomozygous112702207
47075687370756874CT48GENIChomozygous112702209
47075705070757051AC40GENIChomozygous112702211
47075705370757054TC41GENIChomozygous112702213
47075715670757157CT34GENIChomozygous112702215
47075742770757428CA59GENIChomozygous112702217
47075743970757440GA65GENIChomozygous112702219
47075747270757473CT54GENIChomozygous112702221
47075781270757813CT55GENIChomozygous112702231
47075782570757826TG53GENIChomozygous112702233
47075785470757855TA52GENIChomozygous112702235
47075787170757872AG56GENIChomozygous112702237
47075787670757877GA55GENIChomozygous112702239
47075819470758195AT42GENIChomozygous112702241
47075828370758284AC38GENIChomozygous112702243
47075859170758592CT37GENIChomozygous112702245
47075861170758612CA30GENIChomozygous112702247
47075911470759115TA32GENIChomozygous112702251
47075917370759174GT28GENIChomozygous112702253
47075920070759201AG30GENIChomozygous112702255