| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137866935-137867266 | Rare:77 | ||||
| chr6:138773334-138773547 | Common:2; Rare:95 | ||||
| chr6:138773689-138773836 | Common:3; Rare:72 | ||||
| chr6:139028210-139028538 | Common:1; Rare:52 | ||||
| chr6:139028554-139028906 | Common:1; Rare:71 | ||||
| chr6:142301822-142302173 | Common:6; Rare:101 | ||||
| chr6:143060683-143061061 | Common:9; Rare:134 | ||||
| chr6:143450654-143451059 | Common:1; Rare:142; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:143511400-143511779 | Common:4; Rare:113; Clinvar:1 | ||||
| chr6:144285171-144285378 | Common:3; Rare:62 | ||||
| chr6:144286108-144286434 | Common:4; Rare:59 | ||||
| chr6:145814735-145814921 | Common:1; Rare:91 | ||||
| chr6:145964044-145964132 | Common:4; Rare:19 | ||||
| chr6:147508485-147508725 | Common:5; Rare:89 | ||||
| chr6:149546015-149546166 | Common:1; Rare:65 |