| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:32469893-32470293 | Common:4; Rare:136 | ||||
| chr18:32470662-32471161 | Common:1; Rare:297 | ||||
| chr18:34493204-34493506 | Common:2; Rare:136; Clinvar (benign):2 | ||||
| chr18:34493722-34494449 | Common:2; Rare:317 | ||||
| chr18:34494352-34494610 | Common:1; Rare:41 | ||||
| chr18:34976701-34977190 | Common:6; Rare:176 | ||||
| chr18:35041178-35041485 | Common:3; Rare:186 | ||||
| chr18:35240845-35241203 | Common:7; Rare:296 | ||||
| chr18:35290138-35290441 | Common:7; Rare:249 | ||||
| chr18:35343820-35344121 | Common:2; Rare:181 | ||||
| chr18:35344369-35344629 | Common:6; Rare:244 | ||||
| chr18:35345268-35345718 | Common:4; Rare:137 | ||||
| chr18:35377245-35377385 | Common:6; Rare:57 | ||||
| chr18:35497539-35497857 | Common:9; Rare:282 | ||||
| chr18:35497866-35498069 | Common:3; Rare:174 |