| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4786334-4786524 | Rare:46 | ||||
| chr17:4789061-4790006 | Common:10; Rare:624 | ||||
| chr17:4795998-4796295 | Common:5; Rare:265 | ||||
| chr17:4796411-4796811 | Common:5; Rare:155 | ||||
| chr17:4806912-4807234 | Common:12; Rare:270 | ||||
| chr17:4807257-4807999 | Common:8; Rare:280 | ||||
| chr17:4833138-4833546 | Common:1; Rare:261 | ||||
| chr17:4833590-4834090 | Common:2; Rare:179 | ||||
| chr17:4899280-4899570 | Common:3; Rare:340; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
| chr17:4939861-4940725 | Common:10; Rare:604 | ||||
| chr17:4947102-4947502 | Common:4; Rare:141 | ||||
| chr17:4947783-4948183 | Common:2; Rare:232 | ||||
| chr17:4948430-4948850 | Common:14; Rare:419 | ||||
| chr17:4948932-4949271 | Common:5; Rare:231 | ||||
| chr17:4949280-4949716 | Common:7; Rare:282 |