| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184711953-184712243 | Common:1; Rare:97 | ||||
| chr3:185282844-185283015 | Common:1; Rare:42 | ||||
| chr3:185498919-185499151 | Rare:84 | ||||
| chr3:185585958-185586388 | Common:1; Rare:105 | ||||
| chr3:185821122-185821305 | Rare:33 | ||||
| chr3:185824942-185825236 | Rare:88 | ||||
| chr3:186567289-186567441 | Common:3; Rare:38 | ||||
| chr3:186783259-186783596 | Common:1; Rare:126 | ||||
| chr3:186806384-186806547 | Rare:49 | ||||
| chr3:187139429-187139587 | Rare:60 | ||||
| chr3:188153771-188153931 | Common:1; Rare:32 | ||||
| chr3:188154060-188154210 | Rare:39 | ||||
| chr3:190322393-190322538 | Common:2; Rare:36 | ||||
| chr3:190513903-190514128 | Common:2; Rare:64 | ||||
| chr3:193593081-193593380 | Rare:97; Clinvar:2; Clinvar (benign):2 |