| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42654386-42654624 | Rare:70 | ||||
| chr3:44632362-44632579 | Rare:56 | ||||
| chr3:47406259-47406405 | Rare:49; Clinvar (benign):1 | ||||
| chr3:49131381-49131604 | Common:1; Rare:73; Clinvar:2 | ||||
| chr3:49132099-49132137 | Rare:7; Clinvar (pathogenic):1 | ||||
| chr3:52481879-52482177 | Common:1; Rare:53 | ||||
| chr3:61560513-61560823 | Common:1; Rare:99 | ||||
| chr3:61560825-61561058 | Common:3; Rare:68 | ||||
| chr3:64684751-64685282 | Rare:101 | ||||
| chr3:66398133-66398366 | Rare:70 | ||||
| chr3:69012785-69013038 | Common:4; Rare:53 | ||||
| chr3:73547888-73547924 | Rare:3 | ||||
| chr3:75435099-75435377 | Common:2; Rare:94 | ||||
| chr3:81761462-81761603 | Common:5; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:99635329-99635588 | Common:1; Rare:35 |