| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2571237-2571611 | Common:5; Rare:99 | ||||
| chr18:2655563-2655975 | Common:5; Rare:164 | ||||
| chr18:3247340-3247530 | Common:1; Rare:55 | ||||
| chr18:3261808-3262236 | Common:6; Rare:136 | ||||
| chr18:3450063-3450180 | Rare:35 | ||||
| chr18:3874229-3874333 | Rare:33 | ||||
| chr18:4455160-4455460 | Common:2; Rare:111 | ||||
| chr18:5296907-5296997 | Common:1; Rare:29 | ||||
| chr18:6729788-6729923 | Rare:37 | ||||
| chr18:9102523-9102766 | Common:1; Rare:100; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136136-9136352 | Common:3; Rare:66 | ||||
| chr18:9136598-9137042 | Rare:165 | ||||
| chr18:9615032-9615152 | Common:1; Rare:32 | ||||
| chr18:9615198-9615305 | Rare:16 | ||||
| chr18:9914198-9914284 | Rare:43 |