| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76353608-76353677 | Rare:28 | ||||
| chr17:76493138-76493154 | Rare:3 | ||||
| chr17:76537922-76538056 | Rare:52 | ||||
| chr17:76725729-76726094 | Common:1; Rare:103 | ||||
| chr17:76726465-76726872 | Common:5; Rare:151 | ||||
| chr17:76737317-76737529 | Common:3; Rare:82 | ||||
| chr17:76737875-76738043 | Common:3; Rare:48 | ||||
| chr17:77127780-77127879 | Rare:19 | ||||
| chr17:77128114-77128172 | Rare:9 | ||||
| chr17:77129847-77130131 | Common:1; Rare:44 | ||||
| chr17:77320025-77320329 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78130637-78130800 | Rare:31 | ||||
| chr17:78187045-78187406 | Common:3; Rare:122 | ||||
| chr17:78782209-78782572 | Common:9; Rare:122 | ||||
| chr17:78840745-78841082 | Common:2; Rare:127 |