| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158105739-158105893 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158801960-158802155 | Common:2; Rare:90 | ||||
| chr3:160399170-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399512-160399675 | Rare:36 | ||||
| chr3:160449696-160449969 | Common:2; Rare:92 | ||||
| chr3:160565541-160565784 | Common:2; Rare:90 | ||||
| chr3:161221217-161221335 | Common:1; Rare:35 | ||||
| chr3:167734835-167735227 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735617-167735752 | Rare:34 | ||||
| chr3:169773331-169773429 | Rare:31 | ||||
| chr3:169966711-169966843 | Rare:57 | ||||
| chr3:170181717-170181835 | Rare:44 | ||||
| chr3:170908583-170908843 | Common:1; Rare:74 | ||||
| chr3:172711063-172711396 | Common:1; Rare:77 | ||||
| chr3:172750560-172750794 | Common:3; Rare:67 |