| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7403992-7404458 | Common:3; Rare:226 | ||||
| chr17:7404806-7404963 | Common:3; Rare:58 | ||||
| chr17:7435372-7436080 | Common:11; Rare:297 | ||||
| chr17:7479342-7479807 | Common:9; Rare:211 | ||||
| chr17:7483817-7484660 | Common:17; Rare:629 | ||||
| chr17:7484625-7485016 | Common:1; Rare:277 | ||||
| chr17:7485029-7485429 | Common:6; Rare:106 | ||||
| chr17:7558129-7558388 | Common:2; Rare:120 | ||||
| chr17:7561701-7562080 | Common:6; Rare:251 | ||||
| chr17:7572359-7572949 | Common:1; Rare:246 | ||||
| chr17:7573595-7573995 | Common:3; Rare:245 | ||||
| chr17:7576251-7576832 | Common:4; Rare:218 | ||||
| chr17:7577011-7577546 | Common:2; Rare:243 | ||||
| chr17:7579335-7579971 | Common:3; Rare:322 | ||||
| chr17:7583478-7583936 | Common:3; Rare:503; Clinvar:12; Clinvar (benign):14; Clinvar (pathogenic):3 |