chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366668150366669TG17GENIChomozygous114056068
5150366695150366696GC20GENIChomozygous114056069
5150367422150367423GA20GENIChomozygous114056071
5150369249150369250AG27GENIChomozygous114056077
5150369534150369535TC26GENIChomozygous114056079
5150371883150371884GA29GENIChomozygous114056081
5150375467150375468TC26GENIChomozygous114056085
5150375472150375473CA27GENIChomozygous114056087
5150376116150376117TC23GENIChomozygous114056089
5150377210150377211CT18GENIChomozygous114056091
5150377808150377809AG28GENIChomozygous114056093
5150378500150378501TC16GENIChomozygous114056095
5150379516150379517GT32GENIChomozygous114056097
5150382171150382172CT28GENIChomozygous114056100
5150382239150382240AC28GENIChomozygous114056102
5150382615150382616GA18GENIChomozygous114056104
5150383881150383882TC12GENIChomozygous114056106
5150384424150384425AG19GENIChomozygous114056108
5150384758150384759GA23GENIChomozygous114056112
5150384936150384937CT26GENIChomozygous114056114
5150384971150384972CA23GENIChomozygous114056116
5150385068150385069GA13GENIChomozygous114056118
5150385395150385396GA19GENIChomozygous114056120
5150385891150385892GC17GENIChomozygous114056124
5150385969150385970TC18GENIChomozygous114056126
5150389660150389661GA8GENIChomozygous114056128