| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:30622942-30623500 | Common:1; Rare:116; Clinvar:4; Clinvar (benign):6 | ||||
| chr3:30629324-30629413 | Rare:27 | ||||
| chr3:30629912-30629947 | Rare:7 | ||||
| chr3:30631500-30631633 | Common:1; Rare:15 | ||||
| chr3:30645897-30645973 | Rare:13 | ||||
| chr3:30646211-30646392 | Common:1; Rare:33 | ||||
| chr3:30646523-30646583 | Common:1; Rare:7 | ||||
| chr3:30649214-30649529 | Common:6; Rare:47 | ||||
| chr3:30650635-30650925 | Common:2; Rare:43 | ||||
| chr3:30655405-30655431 | Rare:4 | ||||
| chr3:30655442-30655618 | Rare:33 | ||||
| chr3:30658705-30659160 | Common:3; Rare:67 | ||||
| chr3:30660644-30660681 | Common:2; Rare:10 | ||||
| chr3:30664093-30664289 | Common:1; Rare:44 | ||||
| chr3:30666108-30666365 | Common:2; Rare:46 |