| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8249165-8249385 | Common:1; Rare:61 | ||||
| chr17:8254000-8254301 | Common:1; Rare:98 | ||||
| chr17:8295334-8295518 | Common:1; Rare:47 | ||||
| chr17:8435696-8436042 | Common:4; Rare:132 | ||||
| chr17:10697417-10697722 | Common:5; Rare:125; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:10729995-10730128 | Common:3; Rare:29 | ||||
| chr17:11997436-11997620 | Common:3; Rare:63 | ||||
| chr17:13018021-13018284 | Common:5; Rare:68 | ||||
| chr17:14069335-14069587 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:15563439-15563754 | Common:1; Rare:103 | ||||
| chr17:15684207-15684334 | Common:3; Rare:43 | ||||
| chr17:15699442-15699797 | Common:4; Rare:97 | ||||
| chr17:15999590-16000028 | Common:3; Rare:185; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217094-16217253 | Rare:55; Clinvar:1 | ||||
| chr17:16380561-16380829 | Common:4; Rare:74 |