chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224530238224530239TC10GENIChomozygous630882132
4224530352224530353CT18GENICpossibly homozygous630882133
4224532481224532482CT7GENICpossibly homozygous630882134
4224532842224532843GT11GENICheterozygous630882135
4224532946224532947AG19GENICpossibly homozygous630882136
4224533051224533052TC16GENICheterozygous630882137
4224533202224533203AG19GENICpossibly homozygous630882138
4224533344224533345TC12GENICheterozygous630882139
4224534316224534317AG17GENIChomozygous630882140