| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12377040-12377902 | Common:9; Rare:246; Clinvar:1; Clinvar (benign):8 | ||||
| chr18:12407732-12408052 | Common:7; Rare:128 | ||||
| chr18:12419829-12420157 | Common:4; Rare:77 | ||||
| chr18:12420417-12420590 | Common:2; Rare:61 | ||||
| chr18:12420861-12421302 | Rare:94 | ||||
| chr18:12657141-12657226 | Common:1; Rare:24 | ||||
| chr18:12657574-12657637 | Common:1; Rare:9 | ||||
| chr18:12657641-12658226 | Common:7; Rare:192 | ||||
| chr18:12679296-12679450 | Rare:36 | ||||
| chr18:12702172-12702253 | Common:1; Rare:15 | ||||
| chr18:12702258-12702525 | Rare:73 | ||||
| chr18:12702571-12702815 | Common:3; Rare:97 | ||||
| chr18:12702920-12703085 | Common:2; Rare:70 | ||||
| chr18:12703128-12703178 | Common:1; Rare:20 | ||||
| chr18:12703183-12703274 | Common:1; Rare:22 |