| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128795203-128795418 | Common:1; Rare:46; Clinvar (benign):2 | ||||
| chr3:129183828-129184113 | Common:2; Rare:107 | ||||
| chr3:129249545-129249741 | Common:1; Rare:56 | ||||
| chr3:129439765-129440247 | Common:1; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:130746760-130746929 | Common:3; Rare:54 | ||||
| chr3:131026738-131026885 | Common:2; Rare:37 | ||||
| chr3:131381459-131381795 | Common:3; Rare:82 | ||||
| chr3:131502839-131503013 | Common:1; Rare:75 | ||||
| chr3:132659722-132660008 | Common:3; Rare:67 | ||||
| chr3:133661821-133662007 | Rare:43 | ||||
| chr3:134485413-134485766 | Rare:86 | ||||
| chr3:134485947-134486189 | Common:3; Rare:83 | ||||
| chr3:136862021-136862269 | Common:1; Rare:69 | ||||
| chr3:139389557-139389808 | Common:1; Rare:85 | ||||
| chr3:140941646-140941902 | Common:2; Rare:98 |