| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6320474-6320595 | Common:2; Rare:40 | ||||
| chr11:6390065-6390638 | Common:4; Rare:154; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:6391946-6392080 | Common:2; Rare:45; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:6419027-6419284 | Common:3; Rare:66 | ||||
| chr11:6419367-6419557 | Common:1; Rare:60 | ||||
| chr11:6473840-6474146 | Common:1; Rare:94 | ||||
| chr11:6481242-6481686 | Common:5; Rare:161 | ||||
| chr11:6603159-6603411 | Common:2; Rare:69 | ||||
| chr11:6603536-6603820 | Common:4; Rare:88; Clinvar (benign):3 | ||||
| chr11:6612153-6612476 | Common:4; Rare:98 | ||||
| chr11:6612480-6612534 | Common:1; Rare:11 | ||||
| chr11:6612553-6612759 | Common:2; Rare:43 | ||||
| chr11:6617506-6617703 | Rare:55; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:6619214-6619563 | Common:3; Rare:118; Clinvar:3; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:6655317-6655535 | Common:2; Rare:52 |