| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41066174-41066574 | Common:9; Rare:108 | ||||
| chr17:41505516-41506268 | Common:9; Rare:284; Clinvar:2 | ||||
| chr17:41521610-41522010 | Common:2; Rare:124 | ||||
| chr17:41527118-41527859 | Common:2; Rare:213 | ||||
| chr17:41527889-41528623 | Common:12; Rare:559; Clinvar:11 | ||||
| chr17:41688492-41689041 | Common:13; Rare:1014 | ||||
| chr17:41689200-41689713 | Common:24; Rare:845 | ||||
| chr17:41689786-41690186 | Rare:137 | ||||
| chr17:41771650-41772040 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr17:41784535-41785680 | Common:9; Rare:493 | ||||
| chr17:41785630-41786334 | Common:12; Rare:345 | ||||
| chr17:41786370-41786711 | Common:5; Rare:132; Clinvar:5; Clinvar (benign):7 | ||||
| chr17:41786661-41787070 | Common:5; Rare:192; Clinvar (benign):1 | ||||
| chr17:41811526-41812436 | Rare:652 | ||||
| chr17:41812390-41813020 | Common:13; Rare:346; Clinvar:15 |