| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11908274-11908423 | Rare:43 | ||||
| chr18:12307943-12308307 | Common:6; Rare:138 | ||||
| chr18:12658073-12658216 | Common:5; Rare:63 | ||||
| chr18:12702622-12703090 | Common:3; Rare:181 | ||||
| chr18:12947703-12947999 | Common:2; Rare:61 | ||||
| chr18:12991143-12991378 | Common:1; Rare:85 | ||||
| chr18:13726496-13726720 | Common:3; Rare:84 | ||||
| chr18:22933786-22933889 | Common:1; Rare:40 | ||||
| chr18:23453148-23453353 | Rare:72 | ||||
| chr18:23503300-23503547 | Common:2; Rare:91 | ||||
| chr18:23586408-23586537 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24426530-24426765 | Common:5; Rare:96 | ||||
| chr18:35041268-35041459 | Rare:72 | ||||
| chr18:35240917-35241090 | Common:2; Rare:64 | ||||
| chr18:35290156-35290391 | Common:2; Rare:77 |