chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5124574012124574013CT14INTERGENIChomozygous55686034
5124574269124574270CA32INTERGENIChomozygous55686035
5124575013124575014TC28INTERGENIChomozygous55686036
5124575652124575656GTGT----3INTERGENIChomozygous56448439
5124575825124575826CA21INTERGENIChomozygous55686037
5124575914124575915TG18INTERGENIChomozygous55686038
5124576337124576338AG32INTERGENIChomozygous55686039
5124576487124576488GT12INTERGENIChomozygous55686040
5124577290124577291AACCCTCCCCCCAACAATCACATTCACTGCGGTT13INTERGENIChomozygous56353891
5124577862124577865AGT---12INTERGENICheterozygous56579737
5124577867124577879ATACCATGTGTG------------13INTERGENICheterozygous56579738
5124577885124577886T-16INTERGENICheterozygous56579739
5124578397124578398T-6INTERGENICheterozygous56814309
5124580049124580050GT18INTERGENIChomozygous55686045
5124581322124581323GGA19INTERGENICheterozygous55686048
5124583646124583647CCT23INTERGENIChomozygous55686055
5124583684124583685GA29INTERGENIChomozygous55686056
5124583905124583906TG34INTERGENIChomozygous55686057
5124584362124584365TTT---13INTERGENICpossibly homozygous55686058
5124584364124584365T-13INTERGENICheterozygous55686059
5124584579124584580AT21INTERGENIChomozygous55686060
5124584636124584637AC25INTERGENIChomozygous55686061
5124585094124585095CT39INTERGENIChomozygous55686062
5124585211124585212TC22INTERGENIChomozygous55686063
5124586296124586297CA11INTERGENIChomozygous55686064
5124586435124586436T-14INTERGENIChomozygous55686065
5124586581124586583TA--12INTERGENIChomozygous55686066
5124587135124587138AAG---21INTERGENIChomozygous55686071
5124587907124587908TG23INTERGENIChomozygous55686072
5124588316124588329CACAGGCCTTTTT-------------45INTERGENICheterozygous56448444
5124623364124623365TC35INTERGENIChomozygous55686078
5124623774124623775TC32INTERGENIChomozygous55686082
5124623777124623778TC36INTERGENIChomozygous55686083
5124623893124623894GGT30INTERGENICheterozygous55686086
5124623930124623931C-30INTERGENICheterozygous55686087