chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86212267162122672TTG48GENIChomozygous52990011
86212284662122847AAT34GENICpossibly homozygous52990013
86212479062124791TC64GENICpossibly homozygous52990015
86212516762125168GT52GENIChomozygous52990017
86212517462125175GGA42GENIChomozygous52990019
86212572462125725TG55GENIChomozygous52990021
86212676562126766TC61GENIChomozygous52990023
86212725562127256AG41GENICpossibly homozygous52990025
86212725962127260GA39GENICheterozygous52990027
86212760962127610GA63GENIChomozygous52990029
86212763962127640CT60GENIChomozygous52990031
86212818362128184CCTT19GENIChomozygous52668827
86213026762130271GTGT----1GENIChomozygous52990033
86213180962131811GG--13GENICheterozygous52668831
86213271862132719CG48GENIChomozygous52990035
86213285562132856T-9GENICheterozygous52990037
86213301762133018CT62GENIChomozygous52990039
86213360062133601TA88GENIChomozygous52990041
86213434562134346CT43GENIChomozygous52990043
86213451962134520CA59GENICpossibly homozygous52990045
86213620362136204TC62GENIChomozygous52990047
86213771362137714GA62GENIChomozygous52990049
86213804262138043CT57GENIChomozygous52990051
86214030962140310GA83GENICpossibly homozygous52990053
86214109662141097CT62GENIChomozygous52990055
86214189862141899CG25GENICpossibly homozygous52990057
86214197362141974GA14GENICheterozygous52990059
86214197962141980GA14GENICheterozygous52990061
86214198562141986GA10GENICheterozygous52990063
86214220462142205CCTT8GENICpossibly homozygous52668833
86214248562142486CG48GENIChomozygous52990065
86214260962142611AG--58GENIChomozygous52990067
86214264162142642AG60GENIChomozygous52990069
86214343262143433AG44GENIChomozygous52990071
86214430862144309TC48GENIChomozygous52990073
86214555962145560CT57GENIChomozygous52990075
86214565762145658CT42GENIChomozygous52990077