| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23202924-23203214 | Common:1; Rare:101 | ||||
| chr3:23916863-23917177 | Rare:119 | ||||
| chr3:23917611-23918031 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr3:24494717-24495126 | Common:2; Rare:110 | ||||
| chr3:24495158-24495289 | Common:1; Rare:28 | ||||
| chr3:25428106-25428398 | Rare:66 | ||||
| chr3:25428428-25428732 | Common:1; Rare:62 | ||||
| chr3:25783371-25783634 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr3:25790008-25790121 | Common:3; Rare:43 | ||||
| chr3:28348607-28348754 | Rare:34 | ||||
| chr3:28348784-28349182 | Common:3; Rare:126 | ||||
| chr3:29280825-29280994 | Common:2; Rare:38 | ||||
| chr3:29280997-29281655 | Common:14; Rare:128 | ||||
| chr3:30606338-30606546 | Common:1; Rare:53; Clinvar:2 | ||||
| chr3:30606737-30606976 | Common:1; Rare:73; Clinvar:5; Clinvar (benign):6 |