chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366668150366669TG28GENIChomozygous114056068
5150366695150366696GC24GENIChomozygous114056069
5150369249150369250AG28GENIChomozygous114056077
5150369534150369535TC25GENIChomozygous114056079
5150369675150369676TG22GENICpossibly homozygous119021042
5150371883150371884GA21GENIChomozygous114056081
5150375467150375468TC18GENIChomozygous114056085
5150375472150375473CA16GENIChomozygous114056087
5150376116150376117TC19GENIChomozygous114056089
5150377210150377211CT23GENIChomozygous114056091
5150377808150377809AG15GENIChomozygous114056093
5150378500150378501TC24GENIChomozygous114056095
5150379516150379517GT19GENIChomozygous114056097
5150381317150381318TC7GENIChomozygous119021044
5150381918150381919AG19GENICheterozygous114539600
5150382171150382172CT29GENIChomozygous114056100
5150382239150382240AC37GENICpossibly homozygous114056102
5150383881150383882TC10GENIChomozygous114056106
5150384424150384425AG23GENIChomozygous114056108
5150384936150384937CT20GENIChomozygous114056114
5150384971150384972CA17GENIChomozygous114056116
5150385077150385078GA13GENIChomozygous119021046
5150385395150385396GA30GENIChomozygous114056120
5150385891150385892GC14GENIChomozygous114056124
5150385969150385970TC24GENIChomozygous114056126
5150387229150387230CT14GENIChomozygous119021048