| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156817011-156817330 | Not yet | Rare:87 | 407 | ||
| chr3:157174857-157175253 | Not yet | Common:3; Rare:172 | 403 | ||
| chr3:169765029-169765181 | Not yet | Rare:69; Clinvar:3; Clinvar (pathogenic):2 | 179 | ||
| chr3:171874281-171874557 | Not yet | Common:3; Rare:47 | 342 | ||
| chr3:194583859-194584026 | Not yet | Common:11; Rare:61 | 227 | ||
| chr3:195657945-195658099 | Not yet | Common:9; Rare:25 | 189 | ||
| chr3:195990243-195990452 | Not yet | Rare:26 | 214 | ||
| chr3:197627833-197628011 | Not yet | Common:6; Rare:65 | 129 | ||
| chr3:197850988-197851008 | Not yet | Rare:1 | 37 | ||
| chr4:781812-782153 | Not yet | Common:2; Rare:114 | 310 | ||
| chr4:52712223-52712518 | Not yet | Common:4; Rare:75 | 258 | ||
| chr4:76306533-76306758 | Not yet | Rare:63 | 193 | ||
| chr4:77820243-77820401 | Not yet | Rare:64 | 158 | ||
| chr4:78775334-78775571 | Not yet | Common:1; Rare:58 | 372 | ||
| chr4:113959185-113959488 | Not yet | Common:3; Rare:49 | 406 |