| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993071-36993553 | Common:2; Rare:162; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243369 | Common:1; Rare:50 | ||||
| chr3:37994054-37994160 | Rare:30 | ||||
| chr3:38024510-38024664 | Common:1; Rare:57 | ||||
| chr3:38029597-38029771 | Common:1; Rare:33 | ||||
| chr3:38138381-38138701 | Common:2; Rare:93; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051924-39052052 | Common:1; Rare:45 | ||||
| chr3:39107562-39107704 | Common:3; Rare:45 | ||||
| chr3:39383283-39383437 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383549-39383641 | Rare:25; Clinvar:1 | ||||
| chr3:40309470-40309803 | Common:9; Rare:114 | ||||
| chr3:40505923-40506115 | Rare:46 | ||||
| chr3:41962069-41962370 | Common:4; Rare:70 | ||||
| chr3:42581913-42582137 | Common:3; Rare:69 | ||||
| chr3:42600309-42600777 | Common:3; Rare:177 |