| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7576331-7576656 | Common:3; Rare:88 | ||||
| chr17:7583508-7583865 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7627635-7627988 | Common:3; Rare:122 | ||||
| chr17:7687456-7687625 | Rare:37; Clinvar:1 | ||||
| chr17:7857096-7857296 | Common:1; Rare:98 | ||||
| chr17:7857382-7857735 | Common:3; Rare:113 | ||||
| chr17:7857797-7858283 | Common:3; Rare:172 | ||||
| chr17:7885177-7885355 | Rare:58 | ||||
| chr17:7885484-7885842 | Common:4; Rare:74 | ||||
| chr17:7902963-7903401 | Common:2; Rare:95; Clinvar (pathogenic):1 | ||||
| chr17:7931906-7932267 | Common:5; Rare:101 | ||||
| chr17:8151243-8151498 | Common:2; Rare:57 | ||||
| chr17:8162886-8163093 | Rare:72 | ||||
| chr17:8176297-8176510 | Rare:67 | ||||
| chr17:8248029-8248148 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2 |