| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7580772-7580997 | Common:1; Rare:60 | ||||
| chr17:7583542-7583874 | Common:1; Rare:135; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584070-7584347 | Common:1; Rare:62 | ||||
| chr17:7585705-7585993 | Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7627482-7627539 | Common:1; Rare:15 | ||||
| chr17:7627767-7628000 | Common:3; Rare:71 | ||||
| chr17:7650637-7650928 | Common:2; Rare:81 | ||||
| chr17:7686526-7686680 | Rare:42 | ||||
| chr17:7687456-7687560 | Rare:25; Clinvar:1 | ||||
| chr17:7843672-7843749 | Rare:28 | ||||
| chr17:7857100-7857333 | Common:1; Rare:119 | ||||
| chr17:7857459-7858322 | Common:6; Rare:287 | ||||
| chr17:7885195-7885351 | Rare:51 | ||||
| chr17:7931890-7932248 | Common:5; Rare:95 | ||||
| chr17:8210529-8210725 | Common:2; Rare:40 |