chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X115017696115017698AA--3GENICheterozygous45265033
X115022643115022644AG22GENICpossibly homozygous45198328
X115022694115022695CT18GENIChomozygous45198329
X115023319115023320GC13GENIChomozygous45198330
X115023642115023643TG21GENIChomozygous45198331
X115023945115023946AG11GENIChomozygous45198332
X115023994115023995TC2GENIChomozygous45198333
X115025069115025070AG4GENIChomozygous45198352
X115026745115026746GA2GENICheterozygous45198353
X115028217115028218GT19GENIChomozygous45198355
X115028525115028526TC19GENIChomozygous45198361
X115028611115028612GA19GENICpossibly homozygous45198362
X115029541115029542AG15GENIChomozygous45198363
X115031584115031585GA7GENIChomozygous45198364
X115033569115033570CT17GENIChomozygous45198366
X115033610115033611AG15GENIChomozygous45198367
X115033941115033942CT13GENIChomozygous45198368
X115035179115035180TC10GENICheterozygous45198369
X115035511115035512CT17GENICheterozygous45198370
X115035767115035768CT18GENICpossibly homozygous45198371
X115037371115037372AAAG7GENIChomozygous45198375
X115042248115042249TC14GENIChomozygous45198377
X115043250115043251AG27GENIChomozygous45198378
X115043322115043323AG28GENIChomozygous45198379
X115045109115045110GA29GENICpossibly homozygous45198380
X115047086115047087CT6GENIChomozygous45198382
X115049642115049643AC10GENIChomozygous45198384
X115051445115051446CT20GENIChomozygous45198385
X115051499115051500GA10GENIChomozygous45198386
X115053625115053626GA22GENIChomozygous45198387
X115053712115053713TC11GENIChomozygous45198388
X115054401115054402TTC11GENICpossibly homozygous45198389
X115055253115055254GA17GENICpossibly homozygous45198390