| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2400606-2400735 | Rare:38 | ||||
| chr17:2400981-2401464 | Common:1; Rare:142 | ||||
| chr17:2401501-2401815 | Rare:110 | ||||
| chr17:2511099-2511451 | Common:4; Rare:65 | ||||
| chr17:2511459-2511688 | Rare:38 | ||||
| chr17:2511749-2512039 | Common:2; Rare:78 | ||||
| chr17:2512240-2512309 | Common:1; Rare:12 | ||||
| chr17:2593177-2593320 | Rare:38 | ||||
| chr17:2593371-2593796 | Common:5; Rare:147; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:2593934-2594233 | Rare:82; Clinvar:1 | ||||
| chr17:2710966-2711102 | Rare:40 | ||||
| chr17:2711129-2711133 | Common:1 | ||||
| chr17:2711179-2711374 | Common:2; Rare:50 | ||||
| chr17:2711667-2712058 | Common:2; Rare:108 | ||||
| chr17:2712456-2712550 | Common:1; Rare:18 |