| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433500-58433632 | Common:1; Rare:47; Clinvar (benign):2 | ||||
| chr3:58433776-58434110 | Common:2; Rare:240; Clinvar:6; Clinvar (benign):9 | ||||
| chr3:58491620-58492184 | Common:8; Rare:270 | ||||
| chr3:59049786-59050330 | Common:3; Rare:349 | ||||
| chr3:61251318-61251638 | Common:8; Rare:129 | ||||
| chr3:61561346-61561773 | Common:7; Rare:350 | ||||
| chr3:61561868-61562268 | Common:1; Rare:123 | ||||
| chr3:62318785-62319261 | Common:2; Rare:381 | ||||
| chr3:62319897-62320049 | Rare:31 | ||||
| chr3:63863740-63863959 | Common:2; Rare:70 | ||||
| chr3:63911893-63912203 | Rare:154 | ||||
| chr3:63912346-63913199 | Common:7; Rare:510; Clinvar (benign):3 | ||||
| chr3:64012866-64013970 | Common:11; Rare:452 | ||||
| chr3:64017207-64017505 | Common:8; Rare:95 | ||||
| chr3:64023225-64023636 | Common:6; Rare:405 |