chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18597930885979309TC15GENIChomozygous142842935
18597982485979825AG23GENIChomozygous142842936
18598401385984014CT15GENIChomozygous142842937
18598401885984019CT17GENIChomozygous142842938
18598487585984876TC18GENIChomozygous142842939
18598502085985021TC31GENIChomozygous142842940
18598612285986123TA15GENIChomozygous142842941
18598613285986133GA15GENIChomozygous142842942
18598618385986184GA18GENIChomozygous142842943
18598653785986538GA11GENIChomozygous142842944
18598678385986784CT7GENIChomozygous142842945
18598727885987278A9GENIChomozygous143740131
18597990585979905CCTGTACCTGATGTACCTGCAAGTTCCCTGTGCATCTG30GENIChomozygous142790330
18597990985979909CG33GENIChomozygous142790331
18598618285986182T18GENIChomozygous142790332
18598716785987167GTGTGTGTGTGC9GENICheterozygous142790333
18598716585987165GTGT9GENICheterozygous143740129
18598727785987277ATG8GENIChomozygous143740130
18598734585987346TG12GENIChomozygous142842946
18598780785987808CT6GENIChomozygous142842947
18598792585987925AG23GENIChomozygous142790334
18598824285988243GC32GENIChomozygous142842948
18598842285988423GA16GENIChomozygous142842949
18598877785988778GA15GENIChomozygous142842950
18598884085988841AG12GENIChomozygous142842951
18598886885988869TC20GENIChomozygous142842952
18598974785989771CTGCTGCAGCTGCCTCCGTCAGAC18GENIChomozygous142790335
18599112685991126TG18GENIChomozygous142790336
18598030685980307C17GENICheterozygous402951676
18598030685980307CT17GENIChomozygous402951677
18599151585991516TA19GENIChomozygous142842953
18599329385993294CG23GENICpossibly homozygous142842954
18599122885991229TC13GENIChomozygous143785779
18599123085991231TC13GENIChomozygous143785780