chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1236044917236044918CA16GENIChomozygous135838893
1236049579236049580AC11GENICheterozygous402981981
1236049577236049578A11GENIChomozygous402981978
1236049577236049578AC11GENICheterozygous402981979
1236049579236049580A11GENIChomozygous402981980
1236057181236057181ATT19GENIChomozygous135467032
1236061126236061126T13GENIChomozygous135467034
1236058419236058420A22GENIChomozygous135467033
1236055077236055081AGGA13GENIChomozygous135467031
1236061320236061326GGATAA20GENIChomozygous135467035
1236063668236063669TC17GENIChomozygous135838894
1236066274236066275GA18GENIChomozygous135838895
1236067572236067573TG19GENIChomozygous135838896
1236068918236068918T8GENICpossibly homozygous135467036
1236069534236069535AC16GENIChomozygous135838897
1236070255236070256GC24GENIChomozygous135838898
1236070820236070821AT23GENIChomozygous135838899
1236071962236071963CT26GENIChomozygous135838900
1236072240236072241CT28GENIChomozygous135838901
1236072304236072305GT34GENIChomozygous135838902
1236072543236072544A24GENIChomozygous135467037
1236072547236072547CC25GENIChomozygous135467038
1236075679236075680CT24GENIChomozygous135838903
1236077873236077874TA11GENIChomozygous135838904
1236078779236078779T13GENICheterozygous135467039
1236079483236079484CA12GENIChomozygous135838905
1236080842236080842TA17GENIChomozygous135467040
1236082041236082042GA21GENIChomozygous135838906
1236082504236082504A21GENIChomozygous135467041