| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993051-36993620 | Common:2; Rare:205; Clinvar:39; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr3:36993641-36993840 | Rare:80; Clinvar:7; Clinvar (benign):4 | ||||
| chr3:37176069-37176403 | Common:1; Rare:92 | ||||
| chr3:37242921-37243381 | Common:6; Rare:122 | ||||
| chr3:38024481-38024667 | Common:1; Rare:71 | ||||
| chr3:38029621-38029844 | Common:1; Rare:44 | ||||
| chr3:38138521-38138701 | Common:2; Rare:66; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:38649538-38649896 | Common:4; Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39051950-39052056 | Common:1; Rare:39 | ||||
| chr3:39107555-39107711 | Common:3; Rare:49 | ||||
| chr3:39383283-39383727 | Common:3; Rare:100; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:39406555-39406763 | Common:6; Rare:88 | ||||
| chr3:40099992-40100043 | Common:1; Rare:7 | ||||
| chr3:40309440-40309919 | Common:9; Rare:160 | ||||
| chr3:40457201-40457381 | Common:3; Rare:86 |