chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105956672059566721CA30GENIChomozygous116608299
105956699059566991TC14GENIChomozygous116608301
105956704859567049AC18GENIChomozygous116608303
105956705059567050A18GENIChomozygous128820859
105956708659567087GA20GENIChomozygous116608305
105956744759567448GA25GENIChomozygous116608307
105956747659567477GA20GENIChomozygous116608309
105956806959568070AG22GENIChomozygous116608311
105956835959568359TAG17GENIChomozygous128820860
105956836059568361CG17GENIChomozygous116608313
105956836259568363TG17GENIChomozygous116608315
105956879359568794T13GENIChomozygous128820861
105956887659568877CT9GENIChomozygous117219298
105956889359568894T9GENIChomozygous128820862
105956902459569025AG12GENIChomozygous117411109
105956956959569570GA17GENIChomozygous116608317
105956966759569668CT14GENIChomozygous116608319
105957056059570561CA12GENIChomozygous116608321
105957089959570900CT20GENIChomozygous116608323
105957091159570912AG17GENIChomozygous116608325
105957124859571249TC21GENIChomozygous116608327
105957139959571400CT22GENIChomozygous116608329
105957245559572456CT19GENIChomozygous116608333
105957302059573021GA11GENIChomozygous116608335
105957345959573460TC27GENIChomozygous116608337
105957364559573646TC23GENIChomozygous116608339
105957406259574063TC26GENIChomozygous116608341
105957508859575089GA17GENIChomozygous116608343
105957548059575481AG16GENIChomozygous116608345
105957639259576393GA20GENIChomozygous116608347
105957701059577011CT26GENIChomozygous116608349
105957712659577127T19GENIChomozygous128820863
105957734259577343GA11GENIChomozygous116608351
105957878259578783CT19GENIChomozygous116608353
105957880559578806CT23GENIChomozygous116608355
105957886959578870GA22GENIChomozygous116608357
105958007559580076CA22GENIChomozygous116608359
105958014759580148GA24GENIChomozygous116608361
105958051559580516TC25GENIChomozygous116608363
105957208359572084CG17GENIChomozygous116890521