| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39051924-39052073 | Common:1; Rare:54 | ||||
| chr3:39107562-39107716 | Common:3; Rare:49 | ||||
| chr3:39383258-39383443 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383549-39383676 | Rare:29; Clinvar:2 | ||||
| chr3:39406601-39406758 | Common:2; Rare:68 | ||||
| chr3:40309506-40309880 | Common:8; Rare:130 | ||||
| chr3:40387106-40387223 | Common:2; Rare:38 | ||||
| chr3:40457201-40457370 | Common:2; Rare:79 | ||||
| chr3:40477059-40477193 | Common:1; Rare:34 | ||||
| chr3:40505930-40506132 | Rare:45 | ||||
| chr3:40524815-40524970 | Common:1; Rare:42 | ||||
| chr3:41962032-41962347 | Common:4; Rare:78 | ||||
| chr3:42149078-42149386 | Rare:71 | ||||
| chr3:42581913-42582204 | Common:3; Rare:85 | ||||
| chr3:42590678-42590954 | Common:3; Rare:82 |