| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76772819-76773219 | Rare:136 | ||||
| chr17:76868110-76868470 | Common:1; Rare:112 | ||||
| chr17:77088350-77088898 | Common:9; Rare:424 | ||||
| chr17:77088989-77089389 | Common:19; Rare:248 | ||||
| chr17:77127718-77128118 | Common:2; Rare:126 | ||||
| chr17:77128030-77128470 | Common:6; Rare:89 | ||||
| chr17:77140276-77140418 | Rare:59 | ||||
| chr17:77140452-77141054 | Common:20; Rare:793 | ||||
| chr17:77141122-77141651 | Common:7; Rare:200 | ||||
| chr17:77279762-77280162 | Common:2; Rare:99 | ||||
| chr17:77281102-77281502 | Common:18; Rare:555 | ||||
| chr17:77286534-77286934 | Common:7; Rare:97 | ||||
| chr17:77319230-77319689 | Common:21; Rare:488; Clinvar:6; Clinvar (benign):21 | ||||
| chr17:77319726-77319990 | Common:3; Rare:133; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:77320000-77320323 | Common:4; Rare:154; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):3 |