chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83971355939713560CT22GENIChomozygous52963120
83971511239715113GA24GENIChomozygous52963121
83971729539717296CT15GENIChomozygous52963122
83971762139717622TC33GENIChomozygous52591500
83972095839720959AG22GENIChomozygous52591510
83972225439722255AAAC7GENICheterozygous52963123
83972226139722263AC--7GENICheterozygous53569928
83972346239723463GA23GENIChomozygous52963124
83972434539724346A-12GENICpossibly homozygous52963125
83972796639727969CTT---3GENIChomozygous53633409
83972946839729469AG17GENIChomozygous52591523
83972951339729514CCG13GENIChomozygous52591524
83972970239729703CCAT6GENICheterozygous52591526
83972970239729703CCATAT6GENICheterozygous52591527
83973003639730037G-12GENIChomozygous52591529
83973309439733095AT22GENIChomozygous52591541
83973488039734881GGC18GENIChomozygous52591547
83973490539734907GG--21GENIChomozygous53378077
83973490739734908GGAACA20GENIChomozygous53378079
83973491039734911CA21GENIChomozygous52591549