| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130746676-130747076 | Common:15; Rare:362 | ||||
| chr3:130849957-130850664 | Common:7; Rare:212 | ||||
| chr3:130850639-130850783 | Common:2; Rare:34 | ||||
| chr3:130850691-130851091 | Common:1; Rare:99 | ||||
| chr3:130850993-130851133 | Rare:27 | ||||
| chr3:130893717-130894330 | Common:23; Rare:784 | ||||
| chr3:131026470-131027120 | Common:15; Rare:501 | ||||
| chr3:131381445-131381880 | Common:21; Rare:677 | ||||
| chr3:131502325-131502725 | Common:2; Rare:78 | ||||
| chr3:131502750-131503351 | Common:6; Rare:672 | ||||
| chr3:132416762-132417702 | Common:25; Rare:740 | ||||
| chr3:132417781-132418550 | Common:8; Rare:354 | ||||
| chr3:132659308-132659708 | Rare:171; Clinvar:1 | ||||
| chr3:132659673-132661290 | Common:43; Rare:1257; Clinvar:1 | ||||
| chr3:132721912-132723346 | Common:35; Rare:941; Clinvar:80; Clinvar (benign):27; Clinvar (pathogenic):8 |