| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124914585-124915057 | Common:9; Rare:197 | ||||
| chr12:130871755-130872116 | Common:4; Rare:145 | ||||
| chr12:131710811-131711119 | Rare:78 | ||||
| chr12:131949655-131949969 | Common:2; Rare:101 | ||||
| chr12:132084027-132084316 | Common:6; Rare:92 | ||||
| chr12:132687305-132687694 | Common:4; Rare:145; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132828831-132828976 | Common:4; Rare:48 | ||||
| chr12:132887564-132887845 | Rare:78 | ||||
| chr12:132956280-132956413 | Common:1; Rare:28 | ||||
| chr12:132986236-132986442 | Rare:46 | ||||
| chr12:133037220-133037536 | Common:4; Rare:64 | ||||
| chr12:133130232-133130627 | Common:7; Rare:123 | ||||
| chr13:19633359-19633747 | Common:1; Rare:143 | ||||
| chr13:19782918-19783088 | Common:2; Rare:62 | ||||
| chr13:19958458-19958751 | Common:5; Rare:140 |