chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366668150366669TG42GENIChomozygous114056068
5150366695150366696GC38GENIChomozygous114056069
5150367422150367423GA28GENIChomozygous114056071
5150368771150368772CT7GENICheterozygous114056073
5150369249150369250AG32GENIChomozygous114056077
5150369534150369535TC20GENIChomozygous114056079
5150371883150371884GA21GENIChomozygous114056081
5150374234150374235GT2GENIChomozygous119230184
5150374235150374236AG2GENIChomozygous119230185
5150375467150375468TC15GENIChomozygous114056085
5150375472150375473CA15GENIChomozygous114056087
5150376116150376117TC29GENIChomozygous114056089
5150377210150377211CT34GENIChomozygous114056091
5150377808150377809AG19GENIChomozygous114056093
5150378164150378165CT13GENICheterozygous119253749
5150378171150378172CT14GENICheterozygous119253750
5150378500150378501TC20GENIChomozygous114056095
5150379516150379517GT30GENIChomozygous114056097
5150382171150382172CT26GENIChomozygous114056100
5150382239150382240AC32GENIChomozygous114056102
5150382615150382616GA23GENIChomozygous114056104
5150383881150383882TC9GENIChomozygous114056106
5150384424150384425AG23GENIChomozygous114056108
5150384936150384937CT17GENIChomozygous114056114
5150384971150384972CA17GENIChomozygous114056116
5150385068150385069GA23GENIChomozygous114056118
5150385395150385396GA25GENIChomozygous114056120
5150385891150385892GC20GENIChomozygous114056124
5150385969150385970TC28GENIChomozygous114056126
5150379752150379753CT32GENICpossibly homozygous118983791
5150387223150387224AG33GENIChomozygous118983792