| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6651574-6651849 | Common:1; Rare:81 | ||||
| chr17:7012315-7012685 | Rare:128 | ||||
| chr17:7219817-7219956 | Common:3; Rare:65; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7223919-7224179 | Rare:93; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):9 | ||||
| chr17:7234449-7234621 | Rare:88 | ||||
| chr17:7251963-7252274 | Common:1; Rare:118 | ||||
| chr17:7252462-7252692 | Common:2; Rare:94 | ||||
| chr17:7261090-7261234 | Common:1; Rare:38 | ||||
| chr17:7262432-7262668 | Rare:53 | ||||
| chr17:7351626-7351738 | Rare:19 | ||||
| chr17:7352088-7352196 | Rare:32 | ||||
| chr17:7479517-7479709 | Common:1; Rare:31 | ||||
| chr17:7484215-7484370 | Common:1; Rare:61 | ||||
| chr17:7558183-7558309 | Rare:24 | ||||
| chr17:7561796-7561996 | Common:2; Rare:52 |