| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144901406-144901702 | Common:1; Rare:84 | ||||
| chr8:144950811-144950912 | Common:1; Rare:35 | ||||
| chr9:178974-179254 | Common:4; Rare:51 | ||||
| chr9:2015081-2015380 | Common:2; Rare:85 | ||||
| chr9:2016650-2016933 | Common:2; Rare:79 | ||||
| chr9:2017476-2017718 | Rare:75 | ||||
| chr9:2621437-2621806 | Common:4; Rare:147; Clinvar:1 | ||||
| chr9:2622146-2622236 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:2844049-2844329 | Common:5; Rare:103 | ||||
| chr9:4679437-4679840 | Common:1; Rare:178 | ||||
| chr9:4679953-4680043 | Common:1; Rare:29 | ||||
| chr9:4741083-4741402 | Common:6; Rare:150 | ||||
| chr9:5437824-5438042 | Common:2; Rare:70 | ||||
| chr9:5450447-5450577 | Common:5; Rare:47 | ||||
| chr9:5628898-5629235 | Common:1; Rare:162 |