| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11857091-11857621 | Common:1; Rare:132 | ||||
| chr18:11857563-11857707 | Common:1; Rare:33 | ||||
| chr18:11908110-11908747 | Common:9; Rare:422 | ||||
| chr18:11908704-11909104 | Common:3; Rare:113 | ||||
| chr18:11980400-11980740 | Common:17; Rare:140 | ||||
| chr18:11980686-11981188 | Common:15; Rare:392 | ||||
| chr18:11981210-11981510 | Common:12; Rare:193 | ||||
| chr18:12307830-12308324 | Common:20; Rare:508 | ||||
| chr18:12308290-12308620 | Common:17; Rare:249 | ||||
| chr18:12308640-12309160 | Common:7; Rare:282 | ||||
| chr18:12359567-12359967 | Common:11; Rare:186; Clinvar (benign):1 | ||||
| chr18:12376109-12376509 | Common:3; Rare:86 | ||||
| chr18:12376724-12377124 | Common:1; Rare:263; Clinvar (benign):4 | ||||
| chr18:12377050-12377788 | Common:42; Rare:1011; Clinvar:4; Clinvar (benign):38 | ||||
| chr18:12407657-12408057 | Common:26; Rare:455 |