| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:45967243-45967467 | Rare:84 | ||||
| chr18:46098224-46098558 | Common:11; Rare:98; Clinvar (benign):6 | ||||
| chr18:46104135-46104414 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr18:46917442-46917654 | Common:2; Rare:91 | ||||
| chr18:47150427-47150554 | Common:4; Rare:51 | ||||
| chr18:48539005-48539287 | Common:2; Rare:61 | ||||
| chr18:49487062-49487355 | Common:4; Rare:114 | ||||
| chr18:49490452-49490924 | Common:1; Rare:116 | ||||
| chr18:49561879-49562104 | Rare:58 | ||||
| chr18:49813826-49814303 | Common:2; Rare:194 | ||||
| chr18:50266438-50266645 | Common:1; Rare:83 | ||||
| chr18:50281432-50281847 | Common:3; Rare:130 | ||||
| chr18:50287820-50288027 | Common:3; Rare:41 | ||||
| chr18:50374870-50375141 | Common:3; Rare:90 | ||||
| chr18:50878832-50879228 | Common:4; Rare:130 |