| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1516582-1516971 | Common:2; Rare:138 | ||||
| chr17:1716223-1716544 | Common:3; Rare:97 | ||||
| chr17:1762668-1762855 | Common:4; Rare:46 | ||||
| chr17:1829792-1830062 | Common:8; Rare:113 | ||||
| chr17:2030012-2030181 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
| chr17:2303496-2303633 | Rare:50 | ||||
| chr17:2303728-2303987 | Common:2; Rare:97 | ||||
| chr17:2336430-2336551 | Rare:46 | ||||
| chr17:2511806-2511966 | Common:2; Rare:47 | ||||
| chr17:2593512-2593658 | Common:2; Rare:45 | ||||
| chr17:2593875-2593984 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711762-2712031 | Common:2; Rare:75 | ||||
| chr17:3471765-3471870 | Common:5; Rare:35 | ||||
| chr17:3636225-3636501 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr17:3636630-3636790 | Common:1; Rare:39; Clinvar:4; Clinvar (benign):1 |