| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7857117-7857289 | Common:1; Rare:87 | ||||
| chr17:7857383-7857649 | Common:2; Rare:90 | ||||
| chr17:7885517-7885729 | Common:1; Rare:52 | ||||
| chr17:7893509-7893846 | Common:1; Rare:79 | ||||
| chr17:7931906-7932257 | Common:5; Rare:96 | ||||
| chr17:8176353-8176510 | Rare:43 | ||||
| chr17:8248042-8248181 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249180-8249325 | Common:1; Rare:44 | ||||
| chr17:8295358-8295506 | Common:1; Rare:37 | ||||
| chr17:8435696-8436006 | Common:4; Rare:125 | ||||
| chr17:10697470-10697654 | Common:3; Rare:86; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:13017940-13018341 | Common:7; Rare:134; Clinvar (benign):2 | ||||
| chr17:14069318-14069608 | Common:2; Rare:104; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:14300796-14301128 | Common:3; Rare:88 | ||||
| chr17:15684259-15684334 | Common:2; Rare:33 |