| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17303192-17303380 | Common:3; Rare:59 | ||||
| chr17:17476843-17477053 | Common:3; Rare:62 | ||||
| chr17:17496371-17496580 | Common:2; Rare:57 | ||||
| chr17:17591384-17591500 | Rare:37 | ||||
| chr17:17591602-17591940 | Common:1; Rare:96 | ||||
| chr17:17681791-17682350 | Common:8; Rare:225 | ||||
| chr17:17682800-17683033 | Common:3; Rare:73 | ||||
| chr17:17823602-17823868 | Common:5; Rare:111 | ||||
| chr17:17972896-17973326 | Common:12; Rare:147 | ||||
| chr17:18039135-18039447 | Common:5; Rare:83; Clinvar (benign):1 | ||||
| chr17:18087707-18087972 | Rare:63 | ||||
| chr17:18153843-18153971 | Common:3; Rare:42; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:18182958-18183115 | Common:1; Rare:49 | ||||
| chr17:18183207-18183574 | Rare:102 | ||||
| chr17:18183765-18183935 | Rare:76 |