| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31532396-31532664 | Common:4; Rare:75 | ||||
| chr3:31981634-31981776 | Rare:37 | ||||
| chr3:32106374-32106697 | Common:4; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32391716-32391955 | Common:3; Rare:69 | ||||
| chr3:32502747-32502905 | Rare:53 | ||||
| chr3:32570636-32570966 | Common:1; Rare:145 | ||||
| chr3:33277312-33277495 | Common:1; Rare:50 | ||||
| chr3:33440856-33441076 | Common:2; Rare:45 | ||||
| chr3:33798296-33798692 | Common:2; Rare:114 | ||||
| chr3:33798985-33799049 | Rare:22 | ||||
| chr3:36993078-36993563 | Common:2; Rare:165; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243097-37243316 | Common:3; Rare:60 | ||||
| chr3:38024510-38024671 | Common:1; Rare:60 | ||||
| chr3:39051793-39052052 | Common:2; Rare:73 | ||||
| chr3:39107569-39107680 | Common:2; Rare:36 |