| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:77132710-77132897 | Common:1; Rare:60 | ||||
| chr18:79068929-79069523 | Common:10; Rare:249 | ||||
| chr18:79395830-79395947 | Rare:25 | ||||
| chr18:79679317-79679610 | Common:1; Rare:138 | ||||
| chr18:79679701-79679923 | Common:3; Rare:91 | ||||
| chr18:79950718-79950934 | Rare:85 | ||||
| chr18:79964522-79964678 | Common:1; Rare:48 | ||||
| chr18:79988118-79988223 | Rare:33 | ||||
| chr18:79988501-79988789 | Common:4; Rare:104; Clinvar (pathogenic):2 | ||||
| chr18:80033547-80033643 | Rare:33 | ||||
| chr18:80033716-80033794 | Common:1; Rare:17 | ||||
| chr18:80034648-80034769 | Rare:49 | ||||
| chr18:80109145-80109316 | Rare:56 | ||||
| chr18:80247483-80247745 | Common:2; Rare:75 | ||||
| chr19:344750-344991 | Common:4; Rare:91 |