| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137028183-137028540 | Common:1; Rare:158 | ||||
| chr9:137046101-137046281 | Common:2; Rare:49 | ||||
| chr9:137053910-137054290 | Common:3; Rare:195 | ||||
| chr9:137070511-137070820 | Common:4; Rare:120 | ||||
| chr9:137077239-137077535 | Common:2; Rare:82 | ||||
| chr9:137086622-137087112 | Common:2; Rare:330; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:137188538-137188832 | Common:4; Rare:245 | ||||
| chr9:137188917-137189125 | Rare:86 | ||||
| chr9:137200714-137201054 | Common:6; Rare:191 | ||||
| chr9:137205590-137205773 | Common:1; Rare:157 | ||||
| chr9:137240730-137241230 | Common:7; Rare:281 | ||||
| chr9:137255072-137255394 | Common:12; Rare:229 | ||||
| chr9:137277556-137277908 | Common:4; Rare:157 | ||||
| chr9:137423115-137423439 | Common:3; Rare:194 | ||||
| chr9:137459276-137459476 | Common:1; Rare:83 |