chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1269909427269909428CT9GENIChomozygous108643253
1269910700269910701CA4GENIChomozygous120524134
1269914170269914171CT26GENIChomozygous108643254
1269914584269914585CT19GENIChomozygous108788335
1269915037269915038AG16GENIChomozygous108643255
1269915390269915391TC26GENIChomozygous108643256
1269915555269915556AG25GENIChomozygous108643257
1269915561269915562CG24GENIChomozygous108643258
1269915579269915580AG32GENIChomozygous108643259
1269915956269915957TC22GENIChomozygous108643260
1269915967269915968CA21GENIChomozygous108643261
1269916046269916047AG25GENIChomozygous108643262
1269916210269916211CT20GENIChomozygous108643263
1269916431269916432CA30GENIChomozygous108643264
1269916547269916548GT23GENIChomozygous108643266
1269916653269916654CT24GENIChomozygous108643267
1269918267269918268GT10GENIChomozygous108643268
1269926654269926655CT17GENIChomozygous108643269
1269929104269929105CT28GENIChomozygous108643270
1269929393269929394AT21GENIChomozygous108643271
1269931942269931943TC14GENIChomozygous108643272
1269931974269931975AG21GENIChomozygous108643273
1269932427269932428AG17GENIChomozygous108643274
1269932567269932568AG14GENIChomozygous108643275
1269932743269932744CT13GENIChomozygous108643276
1269934296269934297TG18GENIChomozygous108643277
1269934394269934395GA31GENIChomozygous108643278
1269935045269935046TC19GENIChomozygous108643279
1269936686269936687GT15GENIChomozygous108643280
1269936897269936898TC32GENIChomozygous108643281
1269937783269937784AG15GENIChomozygous108643282
1269937897269937898TA12GENIChomozygous108643283
1269938087269938088TC27GENIChomozygous108643284
1269938140269938141CT35GENIChomozygous108643285
1269938450269938451AG18GENIChomozygous108643286
1269938502269938503CT14GENIChomozygous108643287
1269938774269938775GC23GENIChomozygous108643288
1269914582269914583TC19GENIChomozygous109029788