| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25664882-25665111 | Common:2; Rare:77 | ||||
| chr3:25783391-25783640 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:25790007-25790119 | Common:3; Rare:43 | ||||
| chr3:26623878-26624099 | Common:1; Rare:45 | ||||
| chr3:28348771-28349203 | Common:4; Rare:139 | ||||
| chr3:29280831-29281081 | Common:3; Rare:49 | ||||
| chr3:32106418-32106697 | Common:4; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502784-32502910 | Rare:37 | ||||
| chr3:32570702-32570939 | Rare:108 | ||||
| chr3:33097104-33097239 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277303-33277509 | Common:3; Rare:60 | ||||
| chr3:33645228-33645563 | Rare:56 | ||||
| chr3:33659039-33659215 | Common:3; Rare:38 | ||||
| chr3:33659580-33659728 | Rare:39 | ||||
| chr3:33798520-33798686 | Common:2; Rare:60 |