| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8295358-8295506 | Common:1; Rare:37 | ||||
| chr17:8383050-8383332 | Rare:92 | ||||
| chr17:8383576-8383740 | Common:1; Rare:39 | ||||
| chr17:8867639-8867781 | Common:1; Rare:23 | ||||
| chr17:8965626-8965824 | Common:1; Rare:49 | ||||
| chr17:9162455-9162866 | Common:4; Rare:110 | ||||
| chr17:10697417-10697655 | Common:4; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:10729749-10729833 | Rare:45 | ||||
| chr17:10729966-10730099 | Common:3; Rare:33 | ||||
| chr17:11997422-11997594 | Rare:58 | ||||
| chr17:13017941-13018278 | Common:6; Rare:107; Clinvar (benign):2 | ||||
| chr17:13601899-13602031 | Common:2; Rare:36 | ||||
| chr17:14069342-14069608 | Common:2; Rare:97; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:14300796-14301153 | Common:3; Rare:93 | ||||
| chr17:15262460-15262758 | Rare:64 |