| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130712970-130713078 | Rare:34 | ||||
| chr9:131373456-131373671 | Common:1; Rare:50 | ||||
| chr9:131483451-131483686 | Common:1; Rare:45 | ||||
| chr9:134372855-134373109 | Common:1; Rare:51 | ||||
| chr9:134811386-134811599 | Rare:66; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:136547362-136547681 | Common:2; Rare:93 | ||||
| chr9:136659382-136659441 | Common:1; Rare:16 | ||||
| chr9:136670778-136671011 | Common:1; Rare:62 | ||||
| chr9:136839444-136839744 | Common:1; Rare:109 | ||||
| chrM:15925-16257 | |||||
| chrX:2609154-2609462 | Common:1; Rare:101 | ||||
| chrX:11351635-11351855 | Common:3; Rare:29 | ||||
| chrX:15675383-15675478 | Common:4; Rare:13 | ||||
| chrX:15675606-15675744 | Common:1; Rare:31 | ||||
| chrX:16845051-16845175 | Rare:17 |