chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75468192754681928CT32GENIChomozygous138088355
75468366154683662T15GENIChomozygous137953630
75468529354685294AG29GENIChomozygous138088356
75468575154685752TG15GENIChomozygous138088357
75468685154686852TA17GENIChomozygous138088358
75468990554689906TA29GENIChomozygous138088359
75469006754690068TC26GENIChomozygous138088360
75469020454690204TCCA22GENIChomozygous137953631
75469353054693531TC22GENIChomozygous138088361
75469608754696097TCGGGTGTGC19GENIChomozygous137953632
75469698754696988CT20GENIChomozygous138088362
75469855554698556AG22GENIChomozygous138088363
75469998654699987CT26GENIChomozygous138088364
75470154254701543AG14GENIChomozygous138088365
75470206754702068TC13GENIChomozygous138088366
75470242654702427GT29GENIChomozygous138088367
75470308054703081GA23GENIChomozygous138088368
75470309254703093GC22GENIChomozygous138088369
75470328154703282T22GENIChomozygous137953633
75470336554703366GT25GENIChomozygous138088370
75470494554704946TC14GENIChomozygous138088371
75470639554706396C13GENICheterozygous403211255
75469612654696127CT15GENICheterozygous154442676
75469612654696127C15GENIChomozygous403211251
75470639154706392C13GENIChomozygous403211252
75470639154706392CT13GENICheterozygous403211253
75470639554706396CT13GENIChomozygous403211254
75470806954708070TC24GENIChomozygous138088372
75471075654710757TC13GENIChomozygous138088373
75471087354710874AC21GENIChomozygous138088374
75471088454710885C20GENICheterozygous141915677
75471088454710885CA20GENICpossibly homozygous403211262
75470919854709199A14GENIChomozygous137953634
75471679054716790CACT26GENIChomozygous137953635