chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14107767883107767884TC14GENIChomozygous113539508
14107768470107768471CT6GENIChomozygous125951885
14107768752107768753AG11GENIChomozygous113618067
14107770637107770638CA10GENIChomozygous113828092
14107770956107770957TC20GENIChomozygous113828096
14107771110107771111CT13GENIChomozygous125951886
14107772145107772146CT18GENIChomozygous125951887
14107773426107773427CT12GENIChomozygous113618071
14107773435107773436TC14GENIChomozygous113618072
14107773657107773658AG5GENIChomozygous125951888
14107774417107774418TC17GENIChomozygous113828100
14107774712107774713TA12GENIChomozygous113828102
14107775347107775348AC18GENIChomozygous113828104
14107775601107775602CA5GENIChomozygous125951889
14107776309107776310TC12GENIChomozygous113828108
14107777593107777594GT8GENIChomozygous125951890
14107778151107778152GA8GENIChomozygous125951891
14107778163107778164GC5GENICheterozygous125951892
14107778454107778455CG8GENIChomozygous125951893
14107779458107779459CT14GENIChomozygous125951894
14107778137107778138GA13GENIChomozygous113694966
14107775567107775568TA8GENIChomozygous125925631
14107775571107775572GA8GENIChomozygous125925632
14107775574107775575CA8GENIChomozygous125925633