chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1269909427269909428CT18GENIChomozygous108643253
1269914170269914171CT27GENIChomozygous108643254
1269915037269915038AG26GENIChomozygous108643255
1269915390269915391TC68GENIChomozygous108643256
1269915555269915556AG58GENIChomozygous108643257
1269915561269915562CG55GENIChomozygous108643258
1269915579269915580AG56GENIChomozygous108643259
1269915956269915957TC28GENIChomozygous108643260
1269915967269915968CA29GENIChomozygous108643261
1269916046269916047AG29GENIChomozygous108643262
1269916210269916211CT34GENIChomozygous108643263
1269916431269916432CA62GENIChomozygous108643264
1269916512269916513GA50GENICpossibly homozygous108643265
1269916547269916548GT47GENIChomozygous108643266
1269916653269916654CT37GENIChomozygous108643267
1269918267269918268GT22GENIChomozygous108643268
1269926654269926655CT6GENIChomozygous108643269
1269929104269929105CT21GENIChomozygous108643270
1269929393269929394AT10GENIChomozygous108643271
1269931942269931943TC18GENIChomozygous108643272
1269931974269931975AG23GENIChomozygous108643273
1269932427269932428AG11GENIChomozygous108643274
1269932567269932568AG18GENIChomozygous108643275
1269932743269932744CT12GENIChomozygous108643276
1269934296269934297TG43GENIChomozygous108643277
1269934394269934395GA28GENIChomozygous108643278
1269935045269935046TC40GENIChomozygous108643279
1269936686269936687GT19GENIChomozygous108643280
1269936897269936898TC64GENIChomozygous108643281
1269937783269937784AG17GENIChomozygous108643282
1269937897269937898TA17GENIChomozygous108643283
1269938087269938088TC30GENIChomozygous108643284
1269938140269938141CT41GENIChomozygous108643285
1269938450269938451AG40GENIChomozygous108643286
1269938502269938503CT35GENIChomozygous108643287
1269938774269938775GC40GENIChomozygous108643288