| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52455459-52455663 | Common:2; Rare:73 | ||||
| chr3:52534978-52535124 | Common:2; Rare:33 | ||||
| chr3:52536305-52536745 | Common:3; Rare:134 | ||||
| chr3:52685942-52686049 | Common:1; Rare:37 | ||||
| chr3:52705548-52706217 | Common:4; Rare:212 | ||||
| chr3:52770921-52771009 | Common:2; Rare:22 | ||||
| chr3:53347518-53347850 | Common:2; Rare:103 | ||||
| chr3:53891804-53891996 | Common:2; Rare:62 | ||||
| chr3:56557086-56557238 | Common:2; Rare:60 | ||||
| chr3:57079257-57079373 | Common:2; Rare:39 | ||||
| chr3:57227604-57227899 | Common:3; Rare:101 | ||||
| chr3:57556006-57556325 | Rare:77 | ||||
| chr3:57597330-57597787 | Common:5; Rare:135 | ||||
| chr3:57889750-57890088 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr3:58433809-58433939 | Rare:51; Clinvar (benign):2 |