| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636646-3636768 | Common:1; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668506-3668838 | Common:3; Rare:136 | ||||
| chr17:3723767-3723936 | Common:1; Rare:98 | ||||
| chr17:4142954-4143231 | Common:3; Rare:97 | ||||
| chr17:4143602-4143763 | Common:4; Rare:98 | ||||
| chr17:4263936-4264052 | Rare:46 | ||||
| chr17:4555331-4555514 | Common:3; Rare:83 | ||||
| chr17:4704107-4704191 | Rare:46 | ||||
| chr17:4807007-4807195 | Common:4; Rare:62 | ||||
| chr17:4939906-4940373 | Common:2; Rare:138 | ||||
| chr17:4948368-4948732 | Common:4; Rare:145 | ||||
| chr17:4948931-4949177 | Common:2; Rare:85 | ||||
| chr17:4969027-4969308 | Common:2; Rare:57 | ||||
| chr17:5419432-5419737 | Common:2; Rare:136 | ||||
| chr17:5420054-5420202 | Rare:58 |