| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:9644502-9644842 | Common:3; Rare:58 | ||||
| chr17:9645047-9645093 | Rare:7 | ||||
| chr17:9645319-9645610 | Rare:72 | ||||
| chr17:9645974-9646134 | Common:3; Rare:33 | ||||
| chr17:9669490-9669746 | Common:4; Rare:39 | ||||
| chr17:10697116-10697148 | Rare:16 | ||||
| chr17:10697422-10697799 | Common:6; Rare:148; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:11598285-11598496 | Common:1; Rare:53 | ||||
| chr17:11996857-11997201 | Common:3; Rare:84 | ||||
| chr17:11997251-11997686 | Common:3; Rare:150 | ||||
| chr17:12020686-12020920 | Common:2; Rare:96 | ||||
| chr17:12021216-12021419 | Rare:81 | ||||
| chr17:12665786-12665951 | Rare:33 | ||||
| chr17:12789337-12789616 | Common:1; Rare:90 | ||||
| chr17:13017638-13017786 | Common:1; Rare:64; Clinvar (benign):2 |