| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:5122454-5122563 | Rare:22 | ||||
| chr3:8501532-8501950 | Common:3; Rare:153 | ||||
| chr3:9362977-9363140 | Common:1; Rare:56 | ||||
| chr3:9397436-9397750 | Common:1; Rare:113 | ||||
| chr3:9749772-9750018 | Common:1; Rare:84 | ||||
| chr3:9792374-9792604 | Rare:64 | ||||
| chr3:9792681-9793119 | Common:3; Rare:154 | ||||
| chr3:9933514-9933868 | Common:2; Rare:145; Clinvar:3 | ||||
| chr3:10026311-10026477 | Rare:54 | ||||
| chr3:10115585-10115816 | Common:2; Rare:71 | ||||
| chr3:12484365-12484516 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr3:13548983-13549177 | Common:1; Rare:63 | ||||
| chr3:14124713-14125181 | Common:4; Rare:137; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178524-14178866 | Common:2; Rare:177; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651483-14651828 | Rare:105 |