chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138380757083807571CT45GENIChomozygous114416087
138381126883811269TC50GENIChomozygous114416089
138381327283813273GA46GENIChomozygous114416091
138381452283814523CT61GENIChomozygous114416093
138381557483815575CA57GENIChomozygous114416095
138381692183816922TC48GENIChomozygous114416097
138381912283819123AT24GENIChomozygous114416099
138382161383821614GT44GENIChomozygous114416101
138382177683821777GC44GENIChomozygous114416103
138382471483824715GA37GENIChomozygous114416105
138382518483825185CT61GENIChomozygous114416107
138382678083826781GA42GENIChomozygous114416109
138382777383827774GA33GENIChomozygous114416110
138382781583827816CT31GENIChomozygous114416112
138382841683828417TG50GENIChomozygous114416114
138382857883828579TG39GENIChomozygous114416116
138383127583831276AG3GENIChomozygous114416118
138383136683831367TC22GENIChomozygous114416120
138383420883834209GA37GENIChomozygous114416122
138383433183834332AG46GENIChomozygous114416124
138383514083835141AG33GENIChomozygous114416126
138383615483836155AG33GENIChomozygous114416128
138383686283836863TA27GENIChomozygous114416130
138383779883837799CG44GENIChomozygous114416132
138383878383838784TC44GENIChomozygous114416134
138383971383839714GA48GENIChomozygous114416136
138384199383841994CG19GENIChomozygous114416138
138384201083842011CA13GENIChomozygous114416140