| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74212360-74213213 | Common:11; Rare:253 | ||||
| chr17:74213230-74213679 | Common:34; Rare:603 | ||||
| chr17:74430540-74431090 | Common:14; Rare:312 | ||||
| chr17:74431121-74431524 | Common:4; Rare:234 | ||||
| chr17:74431800-74432230 | Common:5; Rare:390 | ||||
| chr17:74442550-74443202 | Common:17; Rare:222 | ||||
| chr17:74466391-74466830 | Rare:215 | ||||
| chr17:74546050-74546350 | Rare:120 | ||||
| chr17:74748339-74748739 | Common:24; Rare:622 | ||||
| chr17:74776236-74776641 | Common:31; Rare:654 | ||||
| chr17:74868365-74868780 | Common:15; Rare:236 | ||||
| chr17:74872920-74873190 | Common:10; Rare:246; Clinvar (pathogenic):3 | ||||
| chr17:74873190-74874189 | Common:37; Rare:823 | ||||
| chr17:74923110-74923510 | Common:4; Rare:237; Clinvar:4 | ||||
| chr17:74923560-74923980 | Common:10; Rare:145 |