| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9362984-9363117 | Common:1; Rare:52 | ||||
| chr3:9397418-9397924 | Common:1; Rare:161 | ||||
| chr3:9792353-9792570 | Rare:62 | ||||
| chr3:9792685-9793124 | Common:3; Rare:155 | ||||
| chr3:9890474-9890655 | Common:2; Rare:68 | ||||
| chr3:9916896-9917154 | Common:3; Rare:60 | ||||
| chr3:9933524-9933910 | Common:3; Rare:152; Clinvar:3 | ||||
| chr3:10026295-10026480 | Rare:62 | ||||
| chr3:10115518-10115730 | Common:4; Rare:78 | ||||
| chr3:11225884-11226027 | Rare:17 | ||||
| chr3:11610456-11610556 | Rare:20 | ||||
| chr3:11643749-11644088 | Common:2; Rare:92 | ||||
| chr3:11719422-11719581 | Rare:50 | ||||
| chr3:12556912-12557148 | Common:5; Rare:83 | ||||
| chr3:12664084-12664331 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 |