| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127937832-127937932 | Common:1; Rare:23; Clinvar:1 | ||||
| chr9:127950700-127951008 | Common:1; Rare:63 | ||||
| chr9:128091253-128091480 | Rare:46 | ||||
| chr9:128098252-128098480 | Common:1; Rare:46 | ||||
| chr9:128160085-128160455 | Common:2; Rare:94 | ||||
| chr9:128191448-128191673 | Rare:65 | ||||
| chr9:128191775-128191840 | Common:1; Rare:14 | ||||
| chr9:128222547-128222821 | Rare:72; Clinvar (benign):1 | ||||
| chr9:128275919-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322576 | Common:1; Rare:54 | ||||
| chr9:128322739-128322924 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128371159-128371425 | Common:1; Rare:101 | ||||
| chr9:128504628-128504793 | Rare:73; Clinvar:5 | ||||
| chr9:128552394-128552622 | Rare:88; Clinvar:1 | ||||
| chr9:128607671-128608034 | Rare:88; Clinvar:6; Clinvar (benign):9 |