| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49561835-49562105 | Common:1; Rare:76 | ||||
| chr18:49813468-49813742 | Rare:63 | ||||
| chr18:49813816-49814114 | Common:1; Rare:122 | ||||
| chr18:49814385-49814408 | Rare:5 | ||||
| chr18:50281352-50281939 | Common:3; Rare:189 | ||||
| chr18:50287636-50287759 | Rare:45 | ||||
| chr18:50287782-50288154 | Common:5; Rare:83 | ||||
| chr18:50288267-50288351 | Common:1; Rare:13 | ||||
| chr18:50374766-50375151 | Common:5; Rare:110 | ||||
| chr18:50375224-50375376 | Rare:33 | ||||
| chr18:50878549-50878765 | Common:2; Rare:51 | ||||
| chr18:50878771-50879260 | Common:5; Rare:155 | ||||
| chr18:50967847-50968235 | Common:1; Rare:123 | ||||
| chr18:51029977-51030308 | Rare:107; Clinvar:3 | ||||
| chr18:51030565-51030793 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):4 |