chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X111800543111800544TA33GENICheterozygous130202199
X111800550111800551GA35GENICheterozygous130202200
X111800573111800574CT34GENICheterozygous130202201
X111800574111800575CT34GENICheterozygous130202202
X111800577111800578GC34GENICheterozygous130202203
X111800589111800590CT34GENICheterozygous130202204
X111800660111800661AC27GENICheterozygous120059955
X111800774111800775AT14GENICheterozygous132439214
X111800780111800781CA12GENICheterozygous132439215
X111800793111800794GA10GENICheterozygous132439216
X111800802111800803GT11GENICheterozygous132439217
X111800812111800813TG13GENICheterozygous120059959
X111800958111800959TG27GENICheterozygous120714708
X111800967111800968CT24GENICheterozygous131248946
X111801081111801082AG22GENICheterozygous130202206
X111800832111800833GA19GENICheterozygous134472845
X111800834111800835AG19GENICheterozygous134472846
X111800978111800979GT20GENICheterozygous134472847
X111801007111801008GA20GENICheterozygous134472848
X111801088111801122TCCTCTTTCTCCACATCCTCTTCAGCACCTGCTG26GENICheterozygous133985627
X111801189111801190GA17GENICheterozygous131566926