| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184314440-184314664 | Common:3; Rare:65 | ||||
| chr3:184361603-184361917 | Rare:71 | ||||
| chr3:184711915-184712273 | Common:2; Rare:114 | ||||
| chr3:185282849-185283037 | Common:1; Rare:45 | ||||
| chr3:185498874-185499174 | Rare:106 | ||||
| chr3:185585967-185586329 | Common:1; Rare:82 | ||||
| chr3:185824882-185825191 | Rare:89 | ||||
| chr3:186567289-186567469 | Common:3; Rare:42 | ||||
| chr3:186665656-186666016 | Common:2; Rare:69 | ||||
| chr3:186783234-186783639 | Common:2; Rare:178 | ||||
| chr3:186806411-186806541 | Rare:41 | ||||
| chr3:188152905-188153028 | Common:1; Rare:20 | ||||
| chr3:188153791-188154010 | Common:1; Rare:40 | ||||
| chr3:188154053-188154227 | Rare:56 | ||||
| chr3:190120313-190120676 | Common:1; Rare:153; Clinvar (pathogenic):1 |