| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156817011-156817330 | Rare:87 | ||||
| chr3:157174857-157175253 | Common:3; Rare:172 | ||||
| chr3:169765029-169765181 | Rare:69; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr3:171874281-171874557 | Common:3; Rare:47 | ||||
| chr3:194583859-194584026 | Common:11; Rare:61 | ||||
| chr3:195657945-195658099 | Common:9; Rare:25 | ||||
| chr3:195990243-195990452 | Rare:26 | ||||
| chr3:197627833-197628011 | Common:6; Rare:65 | ||||
| chr3:197850988-197851008 | Rare:1 | ||||
| chr4:781812-782153 | Common:2; Rare:114 | ||||
| chr4:52712223-52712518 | Common:4; Rare:75 | ||||
| chr4:76306533-76306758 | Rare:63 | ||||
| chr4:77820243-77820401 | Rare:64 | ||||
| chr4:78775334-78775571 | Common:1; Rare:58 | ||||
| chr4:113959185-113959488 | Common:3; Rare:49 |