| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144508937-144509099 | Rare:43 | ||||
| chr8:144792335-144792562 | Common:3; Rare:85 | ||||
| chr8:144852967-144853151 | Rare:68 | ||||
| chr8:145052180-145052487 | Common:10; Rare:79 | ||||
| chr9:214542-214879 | Common:6; Rare:194; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:2017432-2017732 | Common:2; Rare:98 | ||||
| chr9:2621860-2622180 | Common:6; Rare:111; Clinvar:8; Clinvar (benign):3 | ||||
| chr9:2844034-2844314 | Common:5; Rare:106 | ||||
| chr9:3525984-3526091 | Common:1; Rare:44 | ||||
| chr9:3526420-3526535 | Common:2; Rare:60 | ||||
| chr9:4662223-4662348 | Common:2; Rare:48 | ||||
| chr9:4666351-4666575 | Common:3; Rare:58 | ||||
| chr9:4679437-4679845 | Common:1; Rare:178 | ||||
| chr9:4741083-4741364 | Common:4; Rare:130 | ||||
| chr9:4984743-4985118 | Common:1; Rare:135 |