| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49469423-49469823 | Common:3; Rare:123 | ||||
| chr3:49469921-49470434 | Common:7; Rare:434; Clinvar (benign):2 | ||||
| chr3:49470420-49470690 | Rare:156 | ||||
| chr3:49554311-49554500 | Rare:120 | ||||
| chr3:49673696-49674071 | Common:15; Rare:200 | ||||
| chr3:49674173-49675082 | Common:5; Rare:464 | ||||
| chr3:49689447-49689700 | Common:2; Rare:182 | ||||
| chr3:49723286-49723686 | Common:3; Rare:233; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr3:49723802-49724267 | Common:29; Rare:403 | ||||
| chr3:49786427-49786873 | Common:6; Rare:334 | ||||
| chr3:49856464-49856798 | Common:5; Rare:244 | ||||
| chr3:49903826-49904049 | Common:3; Rare:167 | ||||
| chr3:49929320-49929768 | Common:5; Rare:214 | ||||
| chr3:49929748-49930066 | Rare:172 | ||||
| chr3:49939847-49940224 | Common:1; Rare:222 |