chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117120143171201432CT29GENICheterozygous50890375
117120143371201434AAG29GENICheterozygous50890378
117120303671203037TC14GENICheterozygous50890414
117120307271203073TC12GENICheterozygous50890417
117120565971205660CT20GENICheterozygous50890602
117120576771205768GA24GENICheterozygous50890605
117120592371205924AAC8GENICheterozygous50890608
117120808571208086CT16GENICheterozygous50890743
117120827171208272GA17GENICheterozygous50890750
117120833471208335AG29GENICheterozygous50890756
117120833771208338AC29GENICheterozygous50890759
117120858471208585AG30GENICheterozygous50890767
117120859171208592CA26GENICheterozygous50890770
117120859371208594GA26GENICheterozygous50890773
117120860171208602CT28GENICheterozygous50890776
117120861271208613GC25GENICheterozygous50890779
117120863971208640GA25GENICheterozygous50890781
117120864971208650TC30GENICheterozygous50890784
117120869971208700AC27GENICheterozygous50890787
117120870071208701CT27GENICheterozygous51235972
117120875171208752CA31GENICheterozygous50890790
117120880871208809GA35GENICheterozygous50890793
117120881271208813AG35GENICheterozygous50890799
117120896771208968CT25GENICheterozygous50890802
117120901571209016TC25GENICheterozygous50890805
117120921371209214TC20GENICheterozygous50890807
117120931371209314GA24GENICheterozygous50890811
117120932571209326GA19GENICheterozygous50890813
117120945271209453GA16GENICheterozygous50890816
117120946671209467GA17GENICheterozygous50890820
117120947471209475CG17GENICheterozygous50890823
117120953171209532CT23GENICheterozygous50890826
117120960371209604TC31GENICheterozygous50890829
117121003871210039TC16GENICheterozygous50890832
117121180471211805TC15GENICheterozygous50890883
117121199871211999CA26GENICheterozygous50961116
117121249771212498TTG15GENICheterozygous50820977