chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190853330190853331AG22GENIChomozygous109055337
1190853467190853468AT16GENIChomozygous108978094
1190853484190853485TC18GENIChomozygous108978095
1190853534190853549TAACTCAGCCCTAGC22GENIChomozygous131580218
1190853629190853630GT25GENIChomozygous108978096
1190853906190853907AG19GENIChomozygous108466321
1190853971190853972TC24GENIChomozygous108466322
1190857062190857063GC15GENIChomozygous108466326
1190861588190861589GA21GENIChomozygous108466329
1190858308190858309GT18GENIChomozygous109178404
1190861761190861762CT16GENIChomozygous109178406
1190863158190863159CT22GENIChomozygous109178408
1190863642190863643TC18GENIChomozygous108466330
1190865963190865964TC16GENIChomozygous108466333
1190867710190867710TA21GENIChomozygous131580219
1190869500190869501AG19GENIChomozygous109178410
1190870974190870975TA20GENIChomozygous108466339
1190871107190871108GT13GENIChomozygous109178412
1190871583190871584GA21GENIChomozygous109178414
1190871643190871644CT17GENIChomozygous108466341
1190874195190874196AG30GENIChomozygous108466344
1190874274190874275CT29GENIChomozygous108466345
1190875821190875822CT25GENIChomozygous108466348
1190876586190876587TG23GENIChomozygous108466350
1190874591190874592CA36GENIChomozygous108763759
1190874592190874593AG36GENIChomozygous108763760
1190877735190877736TC15GENIChomozygous108466353
1190878936190878936T19GENIChomozygous131580220
1190879738190879739GA16GENIChomozygous109178416
1190879858190879859AG16GENIChomozygous108466361