| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57577352-57577451 | Common:1; Rare:29 | ||||
| chr3:57580543-57580591 | Rare:7 | ||||
| chr3:57972070-57972297 | Common:1; Rare:46 | ||||
| chr3:58010188-58010256 | Rare:11 | ||||
| chr3:58059427-58059507 | Rare:12 | ||||
| chr3:58096007-58096216 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr3:58104864-58105215 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:58118566-58118962 | Rare:81; Clinvar (benign):1 | ||||
| chr3:58142392-58142733 | Rare:81; Clinvar:2 | ||||
| chr3:58249661-58249780 | Rare:16 | ||||
| chr3:58656826-58657015 | Common:2; Rare:38 | ||||
| chr3:58665427-58665675 | Common:2; Rare:48 | ||||
| chr3:61560847-61561053 | Common:3; Rare:61 | ||||
| chr3:61637605-61637678 | Rare:21 | ||||
| chr3:66394082-66394378 | Common:2; Rare:69; Clinvar (benign):1 |