| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14178529-14178866 | Common:2; Rare:175; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402430-14402576 | Rare:38 | ||||
| chr3:14651462-14651807 | Rare:100 | ||||
| chr3:14947347-14947583 | Common:3; Rare:110 | ||||
| chr3:14948340-14948635 | Common:2; Rare:81 | ||||
| chr3:15205932-15206287 | Rare:123 | ||||
| chr3:15427478-15427623 | Common:1; Rare:51 | ||||
| chr3:15601512-15601753 | Common:4; Rare:98 | ||||
| chr3:15795947-15796167 | Common:3; Rare:36 | ||||
| chr3:15859777-15860071 | Common:4; Rare:93 | ||||
| chr3:16264845-16265237 | Common:2; Rare:135 | ||||
| chr3:16513600-16513793 | Common:4; Rare:51 | ||||
| chr3:17739517-17739695 | Rare:38 | ||||
| chr3:19946884-19947415 | Common:8; Rare:195 | ||||
| chr3:20186136-20186565 | Common:7; Rare:130 |