chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X153555542153555543TG12GENIChomozygous971518313
X153598611153598612TG5GENIChomozygous971518314
X153598612153598613CA5GENIChomozygous971518315
X153598653153598654GT3GENIChomozygous971518316
X153598681153598682GT2GENIChomozygous971518317
X153598870153598871CA7GENIChomozygous971518318
X153602136153602137CT15GENIChomozygous971518319
X153602157153602158CT12GENIChomozygous971518320
X153602220153602221CT6GENIChomozygous971518321
X153644980153644981GA12GENIChomozygous971518322
X153645059153645060TA4GENIChomozygous971518323
X153692285153692286GC5GENIChomozygous971518324
X153730959153730960GC20GENICheterozygous971518325
X153730961153730962AG20GENICheterozygous971518326
X153731007153731008TA16GENICheterozygous971518327
X153772165153772166GT6GENIChomozygous971518328
X153808632153808633AG10GENICheterozygous971518329
X153808638153808639CA10GENICheterozygous971518330
X153836513153836514TG5GENIChomozygous971518331