chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X111800573111800574CT12GENICheterozygous130202201
X111800574111800575CT12GENICheterozygous130202202
X111800577111800578GC12GENICheterozygous130202203
X111800589111800590CT12GENICheterozygous130202204
X111800660111800661AC10GENICheterozygous120059955
X111800683111800684GA10GENICheterozygous130202205
X111800691111800692TG10GENICheterozygous120714697
X111801130111801131G6GENICheterozygous131562974
X111801131111801132TA6GENICheterozygous131566924
X111801156111801157AG6GENICheterozygous131566925
X111801189111801190GA4GENICheterozygous131566926
X111800674111800675AG10GENICheterozygous120072237