| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38136485-38136505 | Rare:8 | ||||
| chr3:38138576-38138811 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38165443-38165731 | Common:1; Rare:98 | ||||
| chr3:39051944-39052060 | Common:1; Rare:43 | ||||
| chr3:39107531-39107684 | Common:2; Rare:48 | ||||
| chr3:39153539-39153750 | Common:3; Rare:66 | ||||
| chr3:39383290-39383437 | Common:2; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383561-39383748 | Rare:53; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:39406932-39406996 | Rare:25 | ||||
| chr3:40309506-40309890 | Common:8; Rare:131 | ||||
| chr3:40457201-40457387 | Common:3; Rare:90 | ||||
| chr3:40477083-40477212 | Common:1; Rare:36 | ||||
| chr3:40505945-40506132 | Rare:40 | ||||
| chr3:40524815-40525023 | Common:1; Rare:60 | ||||
| chr3:41199289-41199632 | Common:1; Rare:145 |