chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138960693089606931CA37GENIChomozygous114783526
138960818089608181CG23GENIChomozygous114571921
138960831589608316AG24GENIChomozygous114571922
138960921489609215GT19GENIChomozygous114783528
138960961189609612GA27GENIChomozygous114783530
138960985589609856GA27GENICpossibly homozygous114783532
138961021189610212CT29GENIChomozygous114783534
138961063689610637AG25GENIChomozygous114571926
138961274689612747AG32GENIChomozygous114571928
138961314689613147CA32GENICpossibly homozygous114783536
138961328889613289AG36GENIChomozygous114571931
138961374189613742TC22GENICpossibly homozygous114783538
138961397989613980GT13GENIChomozygous114783540
138961431989614320CG36GENICpossibly homozygous115190041
138961432589614326GA36GENICpossibly homozygous114783542
138961433389614334GT34GENICpossibly homozygous115190043
138961435789614358GT43GENIChomozygous114571939
138961438489614385TC41GENICpossibly homozygous114783544
138961448689614487GT30GENIChomozygous114783546
138961460389614604TC40GENIChomozygous114783548
138961473889614739TC19GENICpossibly homozygous114783550
138961633789616338TG9GENIChomozygous115190045
138961633989616340TG8GENIChomozygous115190047
138961720189617202GA9GENIChomozygous115190049
138961731589617316GA16GENIChomozygous114783552
138961822389618224GA15GENICpossibly homozygous115190050
138961846989618470AG23GENIChomozygous114571949
138961868789618688TC29GENICpossibly homozygous114783556
138962091889620919GC20GENIChomozygous114571955
138962095989620960TA18GENIChomozygous114571956
138962176989621770AG21GENIChomozygous114571962
138962308989623090CT17GENIChomozygous114571965
138962310889623109CT17GENIChomozygous114571967