chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162342694162342695AG28GENIChomozygous108344225
1162343089162343090TC21GENIChomozygous108344227
1162343890162343891AG30GENIChomozygous108344229
1162344446162344447GC21GENIChomozygous108344231
1162344530162344531AG14GENIChomozygous108344233
1162344613162344614GC13GENIChomozygous108951842
1162344616162344617GA12GENIChomozygous108951843
1162344806162344807TC22GENIChomozygous108344239
1162345264162345265TC25GENIChomozygous108344241
1162345298162345299TC18GENIChomozygous108344243
1162345596162345597AG30GENIChomozygous108344245
1162345834162345835TC20GENIChomozygous108344247
1162345900162345901AG20GENIChomozygous108344249
1162346049162346050AG17GENIChomozygous108344251
1162347098162347099GA22GENIChomozygous108344253
1162347227162347228AG22GENIChomozygous108344255
1162347400162347401CT15GENIChomozygous108344257
1162347410162347411CT20GENIChomozygous108344259
1162348936162348937GA28GENIChomozygous108951844
1162348978162348979CT40GENICheterozygous108344261
1162349033162349034GA29GENIChomozygous108344265
1162349126162349127TC25GENIChomozygous108344267
1162349242162349243GA22GENIChomozygous108344269
1162349601162349602TC28GENIChomozygous108951845
1162349965162349966TG24GENIChomozygous108951846
1162350043162350044AG15GENIChomozygous108951847
1162350328162350329GC19GENIChomozygous108344288
1162359349162359350GT24GENICheterozygous108951848