chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123925699539256998GAT---24GENIChomozygous50451848
123926589639265897CT7GENIChomozygous50198026
123926589739265898AT6GENIChomozygous50198028
123926593439265935TTAG3GENIChomozygous50542774
123926593739265938CCAGTGGTAGAGCGCTTGCCTAGCAAGCA1GENIChomozygous50542775
123927193039271931CCTAATAA5INTERGENICheterozygous50542784
123927556739275568TTCACACACACA8GENIChomozygous50571235
123927881139278813AC--5GENIChomozygous50599086
123927950539279507GT--4GENIChomozygous50542790
123927957339279574A-11GENICheterozygous50198047
123928569139285695AGAA----18GENIChomozygous50412818
123928973939289740TTA16GENICheterozygous50542811
123928974039289741A-16GENICheterozygous50198070
123929136339291364AG28GENIChomozygous50198076
123929425339294255AC--6GENIChomozygous50451850
123929446739294468CCTATA8GENICheterozygous50198087
123929449639294497TTATATATATATATA17GENICheterozygous50622153
123929888439298885TTA34GENIChomozygous50198100
123930017539300178CCC---14GENIChomozygous50542821
123930018539300186CA19GENIChomozygous50542822
123930051439300564TCAGATTTCAAAGACCCAAAAGTCCGCCCTCTCCGTCCAGTTCTTTGGGA--------------------------------------------------19GENIChomozygous50899680
123930056739300622CTGAGGCCACCATTTACCCCGCAGTTCCTTCCCTAGGAGCTGGGGGGGATTGGGG-------------------------------------------------------12GENIChomozygous50899681
123930081139300812AG18GENIChomozygous50451852
123930112839301129CT35GENIChomozygous50451853
123930135139301352GGT26GENICpossibly homozygous50451854
123930145739301458GGA7GENICheterozygous50542824
123930162539301626AAAGAGCAGTC22GENIChomozygous50511472
123930247039302471GGCGC13GENIChomozygous50198113