| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8162891-8163093 | Rare:70 | ||||
| chr17:8176333-8176449 | Rare:40 | ||||
| chr17:8248042-8248119 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249180-8249325 | Common:1; Rare:44 | ||||
| chr17:8383144-8383479 | Common:1; Rare:100 | ||||
| chr17:10059761-10059916 | Rare:29 | ||||
| chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:11997412-11997618 | Common:3; Rare:75 | ||||
| chr17:12665960-12666080 | Common:1; Rare:27 | ||||
| chr17:14069440-14069580 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15563460-15563755 | Common:1; Rare:91 | ||||
| chr17:15699500-15699768 | Common:3; Rare:69 | ||||
| chr17:15999598-16000028 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:17281182-17281422 | Rare:91 | ||||
| chr17:17591580-17591926 | Common:2; Rare:98 |