chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172986365172986366C22GENIChomozygous128276778
5172987503172987504GA16GENIChomozygous114093936
5172988477172988478CT15GENIChomozygous114093938
5172989352172989353AT13GENIChomozygous114093940
5172991693172991694AG27GENIChomozygous114093942
5172991729172991730CT25GENIChomozygous114093944
5172992105172992106GA19GENIChomozygous114093946
5172992295172992295ATATGCATGTTAGCATATGCATGTTAGC13GENIChomozygous128276779
5172992565172992566AG24GENIChomozygous114093948
5172993011172993011AG23GENIChomozygous128276780
5172993021172993021ACAG22GENICheterozygous128276781
5172993659172993660GA22GENIChomozygous114093950
5172995926172995927CT14GENIChomozygous114093956
5172995949172995950G10GENIChomozygous128276782
5172996001172996001ACCGAACCCAGGGCCTTGGGCTTCCTAGGTAAGCACTCTACCACTGAGCT2GENIChomozygous128276783
5172996155172996156TC21GENIChomozygous114093958
5172996957172996958AT15GENIChomozygous114093960
5172998767172998768CT25GENIChomozygous114093962
5173001139173001140AG24GENIChomozygous114093964
5173001394173001395G21GENIChomozygous128276784
5173002434173002438ATAC13GENICheterozygous128276785
5173002512173002530TGGTTGTGAGCCACCGTG26GENIChomozygous128276786
5173002596173002597AG20GENIChomozygous114093966
5173003473173003474CT21GENIChomozygous114093968
5173005567173005568CG16GENIChomozygous114093970
5173005822173005823AG13GENICheterozygous132308632
5173005836173005837TC15GENICheterozygous133824828
5173005854173005855AG11GENICheterozygous129924499
5173006353173006353G31GENIChomozygous128276787
5173007199173007200AG24GENIChomozygous114093972
5173008879173008880GA27GENIChomozygous114093974
5173010201173010202AT21GENIChomozygous114093976
5173014454173014455GA20GENIChomozygous114093978
5173015291173015292AG27GENIChomozygous114093980