| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:43115578-43115899 | Common:2; Rare:73 | ||||
| chr18:43277246-43277659 | Rare:106; Clinvar:1 | ||||
| chr18:44680700-44681006 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967261-45967465 | Rare:74 | ||||
| chr18:46098239-46098595 | Common:11; Rare:99; Clinvar (benign):5 | ||||
| chr18:46104135-46104415 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr18:46173784-46174086 | Common:2; Rare:73 | ||||
| chr18:46333810-46333980 | Common:1; Rare:47 | ||||
| chr18:46917323-46917647 | Common:3; Rare:137 | ||||
| chr18:47150450-47150546 | Common:2; Rare:34 | ||||
| chr18:48539007-48539287 | Common:2; Rare:61 | ||||
| chr18:48539926-48540006 | Rare:10 | ||||
| chr18:49487045-49487343 | Common:3; Rare:115 | ||||
| chr18:49561879-49562086 | Rare:53 | ||||
| chr18:49813825-49814220 | Common:1; Rare:166 |