| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33271639-33272167 | Common:4; Rare:187 | ||||
| chr6:33275789-33276188 | Common:1; Rare:92 | ||||
| chr6:33277057-33277166 | Common:2; Rare:32 | ||||
| chr6:33288985-33289093 | Rare:40 | ||||
| chr6:33289187-33289644 | Common:4; Rare:100 | ||||
| chr6:33298908-33299064 | Rare:41 | ||||
| chr6:33299420-33299510 | Common:1; Rare:21 | ||||
| chr6:33314032-33314109 | Common:2; Rare:28 | ||||
| chr6:33314203-33314513 | Common:4; Rare:44 | ||||
| chr6:33320188-33320530 | Common:2; Rare:103; Clinvar (pathogenic):1 | ||||
| chr6:33391594-33391895 | Common:1; Rare:68 | ||||
| chr6:33410887-33411072 | Rare:37 | ||||
| chr6:33417864-33417980 | Rare:48 | ||||
| chr6:33418020-33418500 | Common:3; Rare:114 | ||||
| chr6:33420037-33420301 | Rare:55; Clinvar (benign):1 |