chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143066632143066633AG28GENIChomozygous572484248
4143067173143067174TA24GENIChomozygous572484249
4143067462143067463AG15GENIChomozygous572484250
4143067524143067525CT19GENIChomozygous572484251
4143067604143067605CT33GENIChomozygous572484252
4143068021143068022AG30GENIChomozygous572484253
4143068398143068399CT21GENIChomozygous572484254
4143068696143068697AG24GENIChomozygous572484255
4143068742143068743AG30GENIChomozygous572484256
4143068861143068862AG27GENIChomozygous572484257
4143068972143068975TTT---9GENIChomozygous714122264
4143069122143069123GA19GENIChomozygous572484258
4143069164143069165CT25GENIChomozygous572484259
4143069285143069286GT22GENICpossibly homozygous572484260
4143069345143069346GA21GENIChomozygous572484261
4143069379143069380GC24GENICpossibly homozygous572484262
4143069523143069524AC14GENIChomozygous572484263
4143071303143071304GT18GENIChomozygous572484264
4143071742143071743AC25GENIChomozygous572484265
4143072361143072362CT37GENIChomozygous575111209
4143072689143072690GA16GENIChomozygous572484266