| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180278705-180278932 | Rare:41 | ||||
| chr3:182682336-182682772 | Common:1; Rare:88 | ||||
| chr3:182717319-182717405 | Rare:20 | ||||
| chr3:182729896-182730122 | Common:2; Rare:40 | ||||
| chr3:182730229-182730395 | Common:2; Rare:33 | ||||
| chr3:182794463-182794507 | Rare:6 | ||||
| chr3:182795460-182795568 | Common:1; Rare:12 | ||||
| chr3:183285906-183286109 | Common:3; Rare:37 | ||||
| chr3:183447393-183447685 | Common:3; Rare:76 | ||||
| chr3:183647947-183648113 | Common:1; Rare:40 | ||||
| chr3:183699627-183699662 | Common:1; Rare:7 | ||||
| chr3:184006086-184006147 | Rare:12 | ||||
| chr3:184250348-184250502 | Common:1; Rare:33 | ||||
| chr3:184710995-184711452 | Common:4; Rare:157; Clinvar (benign):1 | ||||
| chr3:185175548-185175681 | Rare:28 |