| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31036708-31036781 | Common:1; Rare:10 | ||||
| chr18:31041931-31042119 | Common:1; Rare:41 | ||||
| chr18:31058638-31058953 | Common:5; Rare:46 | ||||
| chr18:31091934-31092295 | Common:1; Rare:78; Clinvar:8; Clinvar (benign):6 | ||||
| chr18:31093603-31093680 | Rare:28; Clinvar:1; Clinvar (benign):4 | ||||
| chr18:31139869-31140092 | Common:2; Rare:63 | ||||
| chr18:31203511-31203673 | Common:1; Rare:37 | ||||
| chr18:31206885-31207225 | Common:3; Rare:70 | ||||
| chr18:31249286-31249553 | Rare:45 | ||||
| chr18:31256057-31256205 | Rare:28 | ||||
| chr18:31450470-31450494 | Common:3; Rare:6 | ||||
| chr18:31451048-31451085 | Common:1; Rare:2 | ||||
| chr18:31451753-31451847 | Common:1; Rare:10 | ||||
| chr18:31456196-31456474 | Common:2; Rare:48 | ||||
| chr18:31460129-31460381 | Common:1; Rare:39 |