| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40309496-40309811 | Common:9; Rare:109 | ||||
| chr3:40477091-40477179 | Common:1; Rare:24 | ||||
| chr3:42013550-42013802 | Common:5; Rare:75 | ||||
| chr3:42581874-42582184 | Common:3; Rare:97 | ||||
| chr3:42600494-42600709 | Common:1; Rare:85 | ||||
| chr3:43690809-43690957 | Common:1; Rare:68; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477637-44477695 | Rare:15 | ||||
| chr3:44624844-44625075 | Common:2; Rare:65 | ||||
| chr3:44761600-44761809 | Common:3; Rare:73 | ||||
| chr3:44861772-44861925 | Common:2; Rare:68 | ||||
| chr3:44976113-44976283 | Common:2; Rare:71 | ||||
| chr3:46979517-46979852 | Common:2; Rare:85; Clinvar:1 | ||||
| chr3:48301365-48301492 | Common:1; Rare:27 | ||||
| chr3:48440039-48440276 | Common:1; Rare:72 | ||||
| chr3:48847684-48847982 | Common:1; Rare:85 |