chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366668150366669TG29GENIChomozygous114056068
5150366695150366696GC30GENIChomozygous114056069
5150367422150367423GA38GENIChomozygous114056071
5150369249150369250AG41GENIChomozygous114056077
5150369534150369535TC29GENIChomozygous114056079
5150370454150370455CA2GENIChomozygous119204367
5150371883150371884GA18GENIChomozygous114056081
5150375467150375468TC17GENIChomozygous114056085
5150375472150375473CA19GENIChomozygous114056087
5150376116150376117TC39GENIChomozygous114056089
5150377210150377211CT65GENIChomozygous114056091
5150377808150377809AG30GENIChomozygous114056093
5150378500150378501TC24GENIChomozygous114056095
5150379516150379517GT22GENIChomozygous114056097
5150381919150381920AG14GENICpossibly homozygous118913516
5150382171150382172CT34GENIChomozygous114056100
5150382239150382240AC35GENIChomozygous114056102
5150382615150382616GA47GENICpossibly homozygous114056104
5150383881150383882TC4GENIChomozygous114056106
5150384424150384425AG47GENIChomozygous114056108
5150384758150384759GA19GENIChomozygous114056112
5150384936150384937CT35GENIChomozygous114056114
5150384971150384972CA24GENIChomozygous114056116
5150385068150385069GA18GENIChomozygous114056118
5150385891150385892GC13GENIChomozygous114056124
5150385969150385970TC20GENIChomozygous114056126
5150389660150389661GA63GENIChomozygous114056128
5150379752150379753CT20GENIChomozygous118983791
5150387223150387224AG8GENIChomozygous118983792