| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946972-19947310 | Common:5; Rare:126 | ||||
| chr3:23916905-23917196 | Rare:111 | ||||
| chr3:25428106-25428346 | Rare:52 | ||||
| chr3:25783390-25783640 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25790008-25790108 | Common:2; Rare:38 | ||||
| chr3:28348600-28348700 | Rare:19 | ||||
| chr3:28348779-28348884 | Common:1; Rare:28 | ||||
| chr3:28348994-28349185 | Common:2; Rare:54 | ||||
| chr3:29280837-29281102 | Common:3; Rare:55 | ||||
| chr3:32502787-32502956 | Rare:42 | ||||
| chr3:32570718-32570966 | Common:1; Rare:110 | ||||
| chr3:33277325-33277489 | Common:1; Rare:42 | ||||
| chr3:33798380-33798700 | Common:2; Rare:101 | ||||
| chr3:33798997-33799163 | Rare:52 | ||||
| chr3:36993124-36993550 | Common:2; Rare:131; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):2 |