| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7857869-7858063 | Rare:68 | ||||
| chr17:7931906-7932235 | Common:5; Rare:90 | ||||
| chr17:8162881-8163087 | Common:1; Rare:71 | ||||
| chr17:8176327-8176441 | Rare:38 | ||||
| chr17:8248042-8248119 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8965658-8965783 | Common:1; Rare:36 | ||||
| chr17:10697417-10697653 | Common:3; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:11997454-11997620 | Common:3; Rare:56 | ||||
| chr17:14069440-14069648 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:15262439-15262656 | Rare:48 | ||||
| chr17:15999598-16000028 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:17496388-17496575 | Common:2; Rare:51 | ||||
| chr17:17591589-17591911 | Common:2; Rare:91 | ||||
| chr17:17823606-17823821 | Common:5; Rare:97 | ||||
| chr17:18039091-18039370 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):1 |