| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7351771-7352211 | Common:1; Rare:214 | ||||
| chr17:7403204-7404044 | Common:23; Rare:338 | ||||
| chr17:7404074-7404418 | Common:2; Rare:138 | ||||
| chr17:7479496-7479743 | Common:2; Rare:77 | ||||
| chr17:7484192-7484428 | Common:4; Rare:198 | ||||
| chr17:7484689-7484868 | Rare:135 | ||||
| chr17:7548620-7549230 | Common:6; Rare:149; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558127-7558336 | Common:1; Rare:71 | ||||
| chr17:7561723-7562086 | Common:5; Rare:192 | ||||
| chr17:7579306-7579660 | Common:1; Rare:117 | ||||
| chr17:7583701-7583880 | Common:2; Rare:161; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr17:7614548-7614680 | Rare:59 | ||||
| chr17:7614737-7615360 | Rare:294 | ||||
| chr17:7627777-7628000 | Common:4; Rare:126 | ||||
| chr17:7686413-7686704 | Rare:71 |