| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74763200-74764250 | Common:5; Rare:260; Clinvar:3 | ||||
| chr17:74776226-74776573 | Common:11; Rare:219 | ||||
| chr17:74871990-74872640 | Common:6; Rare:137; Clinvar:1 | ||||
| chr17:74872863-74873680 | Common:13; Rare:326; Clinvar (pathogenic):1 | ||||
| chr17:74893593-74893825 | Common:13; Rare:135 | ||||
| chr17:75012565-75012717 | Common:2; Rare:68 | ||||
| chr17:75046929-75047277 | Common:4; Rare:214 | ||||
| chr17:75087595-75087992 | Common:10; Rare:171 | ||||
| chr17:75109848-75110010 | Common:4; Rare:100 | ||||
| chr17:75130710-75131172 | Common:5; Rare:269 | ||||
| chr17:75131679-75131860 | Common:5; Rare:153 | ||||
| chr17:75182839-75183216 | Common:3; Rare:240 | ||||
| chr17:75205299-75205759 | Common:2; Rare:285 | ||||
| chr17:75261568-75261969 | Common:8; Rare:272; Clinvar (benign):8 | ||||
| chr17:75271111-75271426 | Common:4; Rare:99 |