chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159389957159389958AG18GENIChomozygous119705327
3159390661159390662AG32GENIChomozygous112369239
3159393413159393414CT24GENIChomozygous112369241
3159393546159393547TC46GENIChomozygous112369242
3159394601159394602TA26GENIChomozygous112369243
3159394785159394786AG22GENIChomozygous112369244
3159395395159395396TC26GENIChomozygous112369245
3159395399159395400TC24GENIChomozygous112369246
3159395418159395419TG24GENIChomozygous112369247
3159397499159397500AG33GENIChomozygous112369248
3159397549159397550AG33GENIChomozygous112369249
3159397571159397572CT37GENIChomozygous112369250
3159397878159397879GA36GENIChomozygous112369251
3159398547159398548CT45GENIChomozygous112369255
3159398688159398689TC39GENIChomozygous112369256
3159399729159399730TC33GENIChomozygous112369257
3159401088159401089TC23GENIChomozygous112369258
3159402220159402221CT32GENIChomozygous112369259
3159405024159405025GC32GENIChomozygous112369260
3159405289159405290TG29GENIChomozygous111789548
3159405752159405753TC31GENIChomozygous112369261
3159408142159408143GT37GENIChomozygous111789556
3159409990159409991TC18GENIChomozygous112369262
3159411058159411059GA20GENICpossibly homozygous112369263
3159413182159413183GA39GENIChomozygous112369264