| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150603096-150603638 | Common:7; Rare:420 | ||||
| chr3:150603759-150604159 | Common:2; Rare:101 | ||||
| chr3:150702788-150703567 | Common:9; Rare:233 | ||||
| chr3:150703600-150704083 | Common:9; Rare:496 | ||||
| chr3:150762758-150763711 | Common:5; Rare:511 | ||||
| chr3:151085000-151085380 | Common:1; Rare:119 | ||||
| chr3:151085479-151085798 | Rare:270 | ||||
| chr3:151086297-151086666 | Common:9; Rare:132 | ||||
| chr3:151086703-151086983 | Common:2; Rare:146 | ||||
| chr3:151316115-151316817 | Common:6; Rare:124 | ||||
| chr3:151316739-151316881 | Common:1; Rare:26 | ||||
| chr3:152268380-152268720 | Common:5; Rare:181; Clinvar (benign):1 | ||||
| chr3:152268717-152269064 | Rare:291 | ||||
| chr3:152269102-152269420 | Rare:183 | ||||
| chr3:152269440-152269730 | Rare:220 |