chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41419530314195304CT48GENIChomozygous113081896
41419573514195736CT57GENIChomozygous112512949
41419589714195898GA36GENICpossibly homozygous113081897
41419661714196618AC60GENICheterozygous112998210
41419662114196622AT59GENICheterozygous113081898
41419665514196656CT48GENICheterozygous112512953
41419681114196812AT26GENIChomozygous112512957
41419721214197213TA28GENICpossibly homozygous112512959
41419755514197556TC40GENICheterozygous113081901
41419789714197898TG17GENICheterozygous112512963
41419790914197910CA24GENICheterozygous113081903
41419806814198069CT53GENIChomozygous112512965
41419813514198136AG43GENICpossibly homozygous112512967
41419863214198633GA62GENICheterozygous113081904
41419886514198866CG27GENICheterozygous113081905
41419893314198934AG24GENICheterozygous112512971
41419906714199068GA62GENICheterozygous113081906
41419918514199186GT41GENICpossibly homozygous113081907
41419937814199379CG59GENICpossibly homozygous113081908
41420000714200008TG153GENICheterozygous112998213
41420006714200068TC67GENICheterozygous113251644
41419666014196661TA43GENICheterozygous113251642
41419666114196662TA42GENICheterozygous113251643
41420011914200120CG43GENICpossibly homozygous113081909
41420030114200302CT57GENICheterozygous113081910
41420067814200679TC83GENICheterozygous113081911
41420104514201046CT36GENIChomozygous113081912
41420113014201131AG59GENICpossibly homozygous112512979
41420166014201661TC25GENIChomozygous112512981
41420166814201669TC27GENIChomozygous112512983