chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366668150366669TG20GENIChomozygous114056068
5150366695150366696GC16GENIChomozygous114056069
5150369249150369250AG27GENIChomozygous114056077
5150369382150369383AG29GENIChomozygous114451097
5150369534150369535TC16GENIChomozygous114056079
5150371883150371884GA29GENIChomozygous114056081
5150374234150374235GT5GENIChomozygous119230184
5150374235150374236AG4GENIChomozygous119230185
5150375415150375416AG22GENIChomozygous114451101
5150375467150375468TC25GENIChomozygous114056085
5150375472150375473CA25GENIChomozygous114056087
5150376116150376117TC10GENIChomozygous114056089
5150376911150376912GC29GENIChomozygous114451103
5150377210150377211CT24GENIChomozygous114056091
5150377808150377809AG20GENIChomozygous114056093
5150378153150378154TC13GENIChomozygous118858844
5150378500150378501TC28GENIChomozygous114056095
5150378996150378997GC27GENIChomozygous114451105
5150379516150379517GT20GENIChomozygous114056097
5150380919150380920GA27GENIChomozygous114451109
5150381920150381921AG17GENIChomozygous118858845
5150382171150382172CT19GENIChomozygous114056100
5150382239150382240AC14GENIChomozygous114056102
5150382642150382643TA28GENIChomozygous114451111
5150384424150384425AG24GENIChomozygous114056108
5150384494150384495AG20GENIChomozygous119230186
5150384936150384937CT40GENIChomozygous114056114
5150384971150384972CA37GENIChomozygous114056116
5150385395150385396GA30GENIChomozygous114056120
5150385891150385892GC14GENIChomozygous114056124
5150385969150385970TC13GENIChomozygous114056126
5150386227150386228GA17GENIChomozygous114451115
5150388934150388935AT14GENIChomozygous114451117
5150389443150389444AC25GENIChomozygous114451119
5150389660150389661GA42GENIChomozygous114056128
5150389859150389860CT19GENIChomozygous114451121