chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA71GENIChomozygous773964245
1263813164263813165CA44GENIChomozygous773964246
1263813492263813493TA39GENIChomozygous773964247
1263814011263814012CT38GENIChomozygous773964248
1263814051263814052CT42GENIChomozygous773964249
1263814338263814339GA48GENIChomozygous773964250
1263815026263815027CT29GENIChomozygous773964251
1263815349263815350GA37GENICpossibly homozygous773964252
1263815744263815745AG43GENIChomozygous773964253
1263817320263817321GA35GENIChomozygous773964254
1263817743263817744AG60GENIChomozygous773964255
1263818715263818716GA23GENIChomozygous773964256
1263819181263819182CT28GENIChomozygous773964257
1263820712263820713TC34GENICpossibly homozygous773964258
1263820813263820814AG30GENIChomozygous773964259
1263820861263820862CT28GENIChomozygous773964260
1263823243263823244CT59GENIChomozygous773964261
1263825226263825227CT41GENICheterozygous773964262
1263825765263825766GT29GENICpossibly homozygous773964263
1263826119263826120GA47GENIChomozygous773964264
1263827331263827332GA37GENIChomozygous773964265
1263828502263828503CA42GENIChomozygous773964266
1263830697263830698GA27GENIChomozygous773964267
1263831722263831723CT19GENICpossibly homozygous773964268
1263832813263832814AG23GENIChomozygous773964269
1263835278263835279CT29GENIChomozygous773964270
1263835926263835927GA16GENIChomozygous773964271
1263840399263840400GA46GENIChomozygous773964272
1263843300263843301AT19GENIChomozygous773964273