| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123712962-123713569 | Rare:201 | ||||
| chr12:123908950-123909350 | Common:10; Rare:124; Clinvar (benign):1 | ||||
| chr12:124188320-124189021 | Common:19; Rare:164 | ||||
| chr12:124191021-124191298 | Common:2; Rare:52 | ||||
| chr12:124232009-124232208 | Rare:40 | ||||
| chr12:124238974-124239233 | Common:3; Rare:45 | ||||
| chr12:124377950-124378436 | Common:5; Rare:230 | ||||
| chr12:124392860-124393752 | Common:10; Rare:310 | ||||
| chr12:124402140-124402620 | Common:4; Rare:234 | ||||
| chr12:124423065-124423378 | Common:5; Rare:124 | ||||
| chr12:124566430-124566829 | Common:1; Rare:190 | ||||
| chr12:124586710-124587220 | Common:9; Rare:170 | ||||
| chr12:124637530-124637980 | Common:6; Rare:134 | ||||
| chr12:124683099-124683553 | Common:11; Rare:203 | ||||
| chr12:124715590-124715870 | Common:5; Rare:81 |