| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149086438-149086735 | Rare:88 | ||||
| chr3:149129542-149129693 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149658002-149658175 | Rare:38 | ||||
| chr3:149752413-149752614 | Common:2; Rare:67 | ||||
| chr3:149813047-149813286 | Common:1; Rare:82 | ||||
| chr3:150603162-150603364 | Common:2; Rare:82 | ||||
| chr3:151085448-151085751 | Rare:109 | ||||
| chr3:151086413-151086683 | Common:5; Rare:73 | ||||
| chr3:152268606-152268950 | Common:2; Rare:131 | ||||
| chr3:152834985-152835158 | Common:2; Rare:56 | ||||
| chr3:154121331-154121451 | Common:2; Rare:54 | ||||
| chr3:154324406-154324573 | Rare:67 | ||||
| chr3:155079331-155079686 | Common:7; Rare:79 | ||||
| chr3:155079829-155080006 | Common:1; Rare:45 | ||||
| chr3:155080187-155080384 | Common:1; Rare:47 |