chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42186580521865806AG25GENIChomozygous937810278
42186638821866389TC33GENIChomozygous937810279
42187078621870787AG35GENIChomozygous937810280
42187155221871553TC27GENIChomozygous937810281
42187217821872179TC31GENIChomozygous937810282
42187241321872414CT15GENIChomozygous937810283
42187260621872607GA24GENIChomozygous937810284
42187577221875773TC21GENIChomozygous937810285
42187810521878106CT38GENIChomozygous937810286
42187947221879473GT23GENIChomozygous937810287
42188121121881212GA28GENIChomozygous937810288
42188223721882238TC18GENIChomozygous937810289
42188234521882346AC27GENIChomozygous937810290
42188360821883609TC25GENIChomozygous937810291
42188639721886398CT17GENIChomozygous937810292
42188652221886523GA26GENIChomozygous937810293
42188661421886615AC19GENIChomozygous937810294
42188758121887582AG25GENIChomozygous937810295
42188801021888011TC22GENIChomozygous937810296
42188836921888370CT23GENIChomozygous937810297
42188970821889709GA29GENIChomozygous937810298
42189231521892316GA37GENIChomozygous937810299
42189328221893283CT28GENIChomozygous937810300
42189334021893341TC25GENIChomozygous937810301
42189397521893976TC28GENIChomozygous937810302
42189692421896925GC42GENIChomozygous937810303