| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7242278-7242586 | Common:1; Rare:105 | ||||
| chr17:7251955-7252321 | Common:1; Rare:146 | ||||
| chr17:7262466-7262723 | Common:3; Rare:61 | ||||
| chr17:7352090-7352207 | Rare:34 | ||||
| chr17:7479490-7479740 | Common:1; Rare:44 | ||||
| chr17:7484203-7484391 | Common:2; Rare:82 | ||||
| chr17:7583535-7583865 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584074-7584113 | Rare:8 | ||||
| chr17:7857382-7857711 | Common:3; Rare:107 | ||||
| chr17:7885182-7885340 | Rare:45 | ||||
| chr17:7885497-7885687 | Rare:41 | ||||
| chr17:7894215-7894513 | Rare:77 | ||||
| chr17:7931906-7932248 | Common:5; Rare:94 | ||||
| chr17:8151191-8151491 | Common:3; Rare:76 | ||||
| chr17:8152367-8152708 | Common:4; Rare:81 |