| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129893514-129893891 | Rare:273 | ||||
| chr3:130746748-130746948 | Common:6; Rare:114 | ||||
| chr3:130893893-130894242 | Common:6; Rare:200 | ||||
| chr3:131026500-131027090 | Common:5; Rare:245 | ||||
| chr3:131381464-131381801 | Common:2; Rare:85 | ||||
| chr3:131502734-131503057 | Common:2; Rare:241 | ||||
| chr3:132417169-132417605 | Common:8; Rare:201 | ||||
| chr3:132659753-132659974 | Common:6; Rare:97 | ||||
| chr3:132722380-132722992 | Common:14; Rare:196; Clinvar:2; Clinvar (benign):4 | ||||
| chr3:133573205-133573775 | Common:11; Rare:253 | ||||
| chr3:133573837-133574037 | Rare:106 | ||||
| chr3:133661500-133662036 | Common:1; Rare:162 | ||||
| chr3:133805352-133805930 | Common:3; Rare:252 | ||||
| chr3:133806210-133806390 | Rare:72 | ||||
| chr3:134250768-134250932 | Common:2; Rare:110 |