| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74148331-74148552 | Common:2; Rare:76 | ||||
| chr18:74291884-74292272 | Common:4; Rare:114 | ||||
| chr18:74496046-74496402 | Common:4; Rare:112 | ||||
| chr18:74597564-74597914 | Common:2; Rare:94 | ||||
| chr18:76822236-76822591 | Common:11; Rare:99 | ||||
| chr18:77087463-77087552 | Common:3; Rare:24 | ||||
| chr18:77133687-77133764 | Rare:18 | ||||
| chr18:79679261-79679548 | Common:1; Rare:144 | ||||
| chr18:79988356-79988640 | Common:3; Rare:104; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:507838-507869 | Common:1; Rare:6 | ||||
| chr19:572328-572661 | Rare:176 | ||||
| chr19:633508-633716 | Common:8; Rare:100 | ||||
| chr19:663118-663421 | Common:3; Rare:119 | ||||
| chr19:859532-859700 | Rare:60 | ||||
| chr19:893143-893506 | Common:3; Rare:167 |