| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17476850-17477025 | Common:3; Rare:46 | ||||
| chr17:17496385-17496519 | Rare:35 | ||||
| chr17:17591386-17591532 | Rare:53 | ||||
| chr17:17823542-17823662 | Common:2; Rare:70 | ||||
| chr17:17836842-17837073 | Common:3; Rare:54 | ||||
| chr17:17972375-17972605 | Common:1; Rare:69 | ||||
| chr17:18039051-18039704 | Common:5; Rare:182; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087816-18087997 | Rare:50 | ||||
| chr17:18183290-18183546 | Rare:69 | ||||
| chr17:18314898-18315197 | Common:1; Rare:79 | ||||
| chr17:18315225-18315337 | Rare:38 | ||||
| chr17:18315707-18316183 | Rare:158 | ||||
| chr17:18363382-18363476 | Common:1; Rare:29 | ||||
| chr17:18781088-18781317 | Common:5; Rare:65 | ||||
| chr17:18856195-18856385 | Common:1; Rare:35 |