| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50611682-50611883 | Rare:48 | ||||
| chr3:51385060-51385336 | Common:1; Rare:84 | ||||
| chr3:51942144-51942442 | Common:2; Rare:78 | ||||
| chr3:51975048-51975143 | Common:1; Rare:35 | ||||
| chr3:52230966-52231225 | Common:1; Rare:70 | ||||
| chr3:52239079-52239255 | Common:2; Rare:64 | ||||
| chr3:52278625-52278781 | Rare:54 | ||||
| chr3:52287759-52287859 | Common:2; Rare:41 | ||||
| chr3:52288012-52288075 | Rare:20 | ||||
| chr3:52451731-52452260 | Rare:133; Clinvar:8; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr3:52452843-52453085 | Common:3; Rare:35 | ||||
| chr3:52455406-52455638 | Common:2; Rare:74 | ||||
| chr3:52685554-52685822 | Common:2; Rare:65 | ||||
| chr3:52685926-52686185 | Common:2; Rare:101 | ||||
| chr3:52705576-52706252 | Common:4; Rare:221 |