chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145095611145095612AT19GENIChomozygous112870611
4145095795145095796AG26GENICpossibly homozygous119412321
4145100240145100241CA27GENIChomozygous112870613
4145100501145100502AG19GENICpossibly homozygous119412322
4145104645145104646AT11GENICheterozygous119587729
4145104650145104651GT11GENICheterozygous119281638
4145104653145104654GT12GENICheterozygous119281640
4145104654145104655AT12GENICheterozygous119454912
4145104785145104786GA13GENIChomozygous112870614
4145104968145104969TC23GENIChomozygous112870615
4145106039145106040TG28GENICpossibly homozygous119412324
4145106184145106185CA32GENICpossibly homozygous112870616
4145107348145107349CT28GENIChomozygous119412325
4145107650145107651AC37GENIChomozygous112870619
4145109472145109473CT24GENIChomozygous119412326
4145110650145110651GA30GENIChomozygous112870624
4145112393145112394CT36GENICpossibly homozygous119587730