chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3113001151113001152TC18INTERGENIChomozygous57996674
3113001252113001253TC16INTERGENICpossibly homozygous57996677
3113002616113002617TC15INTERGENIChomozygous57996680
3113002736113002737CT8INTERGENIChomozygous57996683
3113003848113003849TC13INTERGENIChomozygous57996686
3113004148113004149GA12INTERGENIChomozygous57996689
3113004479113004480AG16INTERGENICpossibly homozygous57603340
3113004777113004778TTATC16INTERGENIChomozygous57996692
3113005013113005014GC37INTERGENIChomozygous57996695
3113005154113005155AT19INTERGENIChomozygous57996698
3113005208113005209TG14INTERGENIChomozygous57996701
3113005275113005276AG17INTERGENIChomozygous57996704
3113005353113005354GT24INTERGENIChomozygous57996707
3113006062113006063GA21INTERGENIChomozygous57996710
3113006065113006069CTGG----17INTERGENIChomozygous57996713
3113006163113006164C-15INTERGENIChomozygous57996717
3113006249113006250CT11INTERGENIChomozygous57996720
3113006303113006304CCT3INTERGENIChomozygous57996723
3113006431113006432GA26INTERGENIChomozygous57996732
3113006554113006555T-23INTERGENIChomozygous57603342
3113006555113006556CCA23INTERGENIChomozygous57603344
3113006993113006994GA13INTERGENIChomozygous57996735
3113007058113007059GA17INTERGENIChomozygous57996738
3113007303113007304AAT17INTERGENIChomozygous57996741
3113007909113007910AG26INTERGENIChomozygous57996743
3113008150113008151T-13INTERGENIChomozygous57996746
3113009208113009209CT9INTERGENIChomozygous57996749
3113029422113029423GA8INTERGENIChomozygous57996755
3113030007113030015GTGTGTGT--------5INTERGENICheterozygous57996758
3113030013113030015GT--5INTERGENICheterozygous57603346
3113030082113030083GGCA12INTERGENICpossibly homozygous57603348
3113031496113031497GA9INTERGENIChomozygous57996762
3113032866113032867TC10INTERGENIChomozygous57996765