| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25428106-25428251 | Rare:26 | ||||
| chr3:25664119-25664350 | Common:2; Rare:75 | ||||
| chr3:25664831-25665170 | Common:4; Rare:108 | ||||
| chr3:25782870-25783149 | Common:1; Rare:61 | ||||
| chr3:25783308-25783640 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:25789875-25790167 | Common:6; Rare:113 | ||||
| chr3:25790295-25790514 | Common:1; Rare:57 | ||||
| chr3:27484174-27484212 | Common:1; Rare:11 | ||||
| chr3:27484260-27484827 | Common:8; Rare:183 | ||||
| chr3:27721853-27722071 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:27722276-27722404 | Rare:40 | ||||
| chr3:28241357-28241815 | Common:2; Rare:149 | ||||
| chr3:28348572-28348887 | Common:1; Rare:79 | ||||
| chr3:28348985-28349252 | Common:3; Rare:88 | ||||
| chr3:29282071-29282209 | Rare:25 |