| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9363001-9363098 | Rare:34 | ||||
| chr3:9397428-9397858 | Common:1; Rare:144 | ||||
| chr3:9749839-9750044 | Common:1; Rare:66 | ||||
| chr3:9750202-9750354 | Common:1; Rare:64 | ||||
| chr3:9792382-9792510 | Rare:37 | ||||
| chr3:9792682-9793124 | Common:3; Rare:155 | ||||
| chr3:9933563-9933863 | Common:1; Rare:115; Clinvar:2 | ||||
| chr3:10026304-10026484 | Rare:57 | ||||
| chr3:10115510-10115702 | Common:4; Rare:69 | ||||
| chr3:10141680-10141850 | Common:1; Rare:76; Clinvar:6; Clinvar (benign):17 | ||||
| chr3:11272233-11272423 | Common:1; Rare:42 | ||||
| chr3:12484323-12484529 | Common:5; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12556967-12557169 | Common:4; Rare:76 | ||||
| chr3:12664075-12664357 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796572-12796672 | Common:3; Rare:27 |