chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366668150366669TG28GENIChomozygous114056068
5150366695150366696GC26GENIChomozygous114056069
5150368791150368792CT6GENIChomozygous114451093
5150368795150368796CT6GENIChomozygous114056075
5150368826150368827AT6GENIChomozygous114451095
5150369249150369250AG23GENIChomozygous114056077
5150369382150369383AG25GENIChomozygous114451097
5150369534150369535TC23GENIChomozygous114056079
5150371883150371884GA33GENIChomozygous114056081
5150375415150375416AG13GENIChomozygous114451101
5150375467150375468TC14GENIChomozygous114056085
5150375472150375473CA14GENIChomozygous114056087
5150376116150376117TC26GENIChomozygous114056089
5150376911150376912GC23GENIChomozygous114451103
5150377210150377211CT29GENIChomozygous114056091
5150377808150377809AG26GENIChomozygous114056093
5150378153150378154TC19GENIChomozygous118858844
5150378500150378501TC28GENIChomozygous114056095
5150378996150378997GC44GENIChomozygous114451105
5150379516150379517GT35GENIChomozygous114056097
5150380232150380233AT7GENIChomozygous114451107
5150380919150380920GA26GENIChomozygous114451109
5150382171150382172CT28GENIChomozygous114056100
5150382239150382240AC28GENIChomozygous114056102
5150382642150382643TA21GENIChomozygous114451111
5150384424150384425AG40GENIChomozygous114056108
5150384936150384937CT23GENIChomozygous114056114
5150384971150384972CA17GENIChomozygous114056116
5150385395150385396GA37GENIChomozygous114056120
5150385891150385892GC17GENIChomozygous114056124
5150385969150385970TC24GENIChomozygous114056126
5150386227150386228GA34GENIChomozygous114451115
5150388934150388935AT24GENIChomozygous114451117
5150389660150389661GA6GENIChomozygous114056128