| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15738409-15738527 | Common:1; Rare:32 | ||||
| chr3:16140444-16140669 | Rare:33 | ||||
| chr3:16140710-16140913 | Rare:33 | ||||
| chr3:16178342-16178447 | Rare:22 | ||||
| chr3:16235122-16235279 | Rare:34 | ||||
| chr3:16358017-16358261 | Common:4; Rare:86 | ||||
| chr3:28347629-28347906 | Common:1; Rare:44 | ||||
| chr3:29283125-29283313 | Rare:38 | ||||
| chr3:30350594-30350737 | Rare:29 | ||||
| chr3:32484038-32484143 | Rare:24 | ||||
| chr3:40453171-40453417 | Common:5; Rare:53 | ||||
| chr3:41201180-41201547 | Common:2; Rare:73 | ||||
| chr3:41225422-41225738 | Rare:67; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:41237795-41238048 | Common:1; Rare:67 | ||||
| chr3:42632349-42632616 | Common:2; Rare:56 |