| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15032440-15032794 | Rare:79 | ||||
| chr3:15065073-15065369 | Common:2; Rare:109 | ||||
| chr3:15099113-15099293 | Rare:45 | ||||
| chr3:15205966-15206322 | Common:1; Rare:129 | ||||
| chr3:15246695-15246884 | Rare:44 | ||||
| chr3:15427471-15427876 | Common:3; Rare:134 | ||||
| chr3:15428068-15428275 | Rare:30 | ||||
| chr3:15601157-15601394 | Common:2; Rare:77 | ||||
| chr3:15601491-15602019 | Common:6; Rare:239; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15797892-15798388 | Common:1; Rare:104 | ||||
| chr3:15859456-15859614 | Common:7; Rare:40 | ||||
| chr3:15859772-15860163 | Common:5; Rare:119 | ||||
| chr3:16264872-16265243 | Common:2; Rare:124 | ||||
| chr3:16513471-16513541 | Rare:21 | ||||
| chr3:16513584-16513873 | Common:4; Rare:75 |