| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:81511905-81512377 | Common:2; Rare:214; Clinvar:8; Clinvar (benign):30; Clinvar (pathogenic):2 | ||||
| chr17:81512713-81513180 | Common:8; Rare:233; Clinvar (benign):14 | ||||
| chr17:81666565-81666768 | Common:1; Rare:89 | ||||
| chr17:81683621-81684052 | Common:5; Rare:232 | ||||
| chr17:81703267-81703489 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr17:81833243-81833382 | Rare:61 | ||||
| chr17:81860958-81861142 | Common:1; Rare:59 | ||||
| chr17:81871303-81871445 | Rare:47 | ||||
| chr17:81937228-81937429 | Rare:72 | ||||
| chr17:81977439-81977642 | Rare:72 | ||||
| chr17:82037683-82037877 | Common:1; Rare:73 | ||||
| chr17:82051593-82051934 | Common:2; Rare:105 | ||||
| chr17:82273385-82273816 | Common:2; Rare:154 | ||||
| chr17:82450726-82450918 | Common:2; Rare:74 | ||||
| chr17:82458483-82458760 | Common:6; Rare:98 |