| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:2015050-2015389 | Common:3; Rare:100 | ||||
| chr9:2017649-2017699 | Rare:12 | ||||
| chr9:2621860-2622169 | Common:4; Rare:101; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:2844047-2844338 | Common:5; Rare:107 | ||||
| chr9:3525751-3526121 | Common:1; Rare:134 | ||||
| chr9:3526409-3526535 | Common:4; Rare:68 | ||||
| chr9:4662223-4662373 | Common:4; Rare:64 | ||||
| chr9:4666388-4666474 | Common:1; Rare:21 | ||||
| chr9:4679437-4679781 | Common:1; Rare:150 | ||||
| chr9:4679797-4679845 | Rare:18 | ||||
| chr9:4679953-4680074 | Common:1; Rare:38 | ||||
| chr9:4741073-4741353 | Common:3; Rare:132 | ||||
| chr9:5437832-5437982 | Common:1; Rare:53 | ||||
| chr9:5450520-5450570 | Common:2; Rare:21 | ||||
| chr9:5628884-5629251 | Common:1; Rare:173 |