chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190853906190853907AG30GENIChomozygous108466321
1190853971190853972TC33GENIChomozygous108466322
1190854812190854813GA19GENIChomozygous120510958
1190855565190855566AG21GENIChomozygous120510959
1190857062190857063GC30GENIChomozygous108466326
1190858189190858190AG37GENIChomozygous120584409
1190859309190859310CT35GENIChomozygous108466327
1190860953190860954AT27GENIChomozygous120584411
1190861588190861589GA30GENIChomozygous108466329
1190862848190862849GA29GENIChomozygous120510960
1190863642190863643TC21GENIChomozygous108466330
1190864706190864707CT21GENIChomozygous120510961
1190865700190865701TA27GENIChomozygous120584413
1190865963190865964TC29GENIChomozygous108466333
1190866153190866154CT39GENIChomozygous108466334
1190866303190866304GA33GENIChomozygous120510962
1190868264190868265AG36GENIChomozygous108466337
1190869466190869467AG43GENIChomozygous120510963
1190870045190870046AT25GENIChomozygous120510964
1190870086190870087GA37GENIChomozygous120510965
1190870144190870145GC24GENIChomozygous120510966
1190870347190870348CT41GENIChomozygous120510967
1190870974190870975TA44GENIChomozygous108466339
1190871028190871029GA28GENIChomozygous120510968
1190871643190871644CT30GENIChomozygous108466341
1190872669190872670AG23GENIChomozygous108466342
1190874195190874196AG25GENIChomozygous108466344
1190874376190874377AC25GENIChomozygous120510969
1190874591190874592CA32GENIChomozygous108763759
1190874592190874593AG32GENIChomozygous108763760
1190874925190874926AT27GENIChomozygous120510970
1190875014190875015TC30GENIChomozygous108466346
1190875821190875822CT35GENIChomozygous108466348
1190876586190876587TG31GENIChomozygous108466350
1190877079190877080TC29GENIChomozygous108466351
1190877461190877462TG38GENIChomozygous108466352
1190877735190877736TC27GENIChomozygous108466353
1190878743190878744AC36GENIChomozygous120510971
1190880299190880300CT28GENIChomozygous120510972