| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633544-123633851 | Common:1; Rare:145; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972580-123972926 | Common:6; Rare:117 | ||||
| chr12:124786473-124786789 | Common:3; Rare:85 | ||||
| chr12:132687305-132687689 | Common:4; Rare:143; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887558-132887810 | Rare:76 | ||||
| chr12:132956260-132956431 | Common:1; Rare:35 | ||||
| chr12:132986172-132986428 | Rare:65 | ||||
| chr12:133130238-133130662 | Common:7; Rare:142 | ||||
| chr13:19782918-19783088 | Common:2; Rare:62 | ||||
| chr13:20773931-20774034 | Rare:34 | ||||
| chr13:21140370-21140621 | Rare:115 | ||||
| chr13:21176491-21176717 | Common:1; Rare:104 | ||||
| chr13:23889297-23889586 | Common:1; Rare:101 | ||||
| chr13:24160509-24160775 | Rare:76 | ||||
| chr13:24512732-24512842 | Common:3; Rare:33 |