| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47930703-47930957 | Rare:134 | ||||
| chr18:47930976-47931378 | Common:1; Rare:275 | ||||
| chr18:47931496-47931701 | Rare:89 | ||||
| chr18:48136798-48136999 | Common:2; Rare:50 | ||||
| chr18:48137021-48137270 | Common:2; Rare:68 | ||||
| chr18:48538927-48539315 | Common:2; Rare:123 | ||||
| chr18:48949260-48949620 | Common:5; Rare:133 | ||||
| chr18:48949680-48950250 | Common:1; Rare:170 | ||||
| chr18:49460530-49460864 | Common:4; Rare:163; Clinvar:7; Clinvar (benign):2 | ||||
| chr18:49487167-49487361 | Common:6; Rare:153 | ||||
| chr18:49813495-49813663 | Rare:74 | ||||
| chr18:49813835-49814335 | Common:3; Rare:338 | ||||
| chr18:50281387-50281914 | Common:3; Rare:290 | ||||
| chr18:50287598-50287749 | Common:1; Rare:86 | ||||
| chr18:50287816-50288180 | Common:10; Rare:126 |