| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383286-39383443 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39406579-39406732 | Common:2; Rare:56 | ||||
| chr3:40309506-40309809 | Common:8; Rare:107 | ||||
| chr3:42581900-42582143 | Common:3; Rare:73 | ||||
| chr3:42600328-42600709 | Common:3; Rare:152 | ||||
| chr3:42804443-42804646 | Common:2; Rare:60 | ||||
| chr3:43690817-43691004 | Common:3; Rare:104; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44477655-44477758 | Common:1; Rare:16 | ||||
| chr3:44761594-44761833 | Common:3; Rare:86 | ||||
| chr3:44976102-44976272 | Common:2; Rare:68 | ||||
| chr3:45712525-45712752 | Common:1; Rare:28 | ||||
| chr3:45995814-45995866 | Rare:13; Clinvar:1 | ||||
| chr3:47380792-47381068 | Rare:85 | ||||
| chr3:47475812-47476088 | Common:3; Rare:110 | ||||
| chr3:48440001-48440307 | Common:3; Rare:113 |