| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130967150-130967395 | Rare:67 | ||||
| chr3:131026720-131026940 | Common:2; Rare:56 | ||||
| chr3:131381489-131381814 | Common:2; Rare:84 | ||||
| chr3:131502829-131503017 | Common:1; Rare:82 | ||||
| chr3:132659792-132659974 | Common:3; Rare:43 | ||||
| chr3:132722090-132722198 | Rare:43; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:133574186-133574281 | Rare:24 | ||||
| chr3:133661837-133662011 | Rare:39 | ||||
| chr3:134250444-134250562 | Common:2; Rare:35 | ||||
| chr3:134250755-134250984 | Common:1; Rare:82 | ||||
| chr3:134485386-134485795 | Rare:102 | ||||
| chr3:134485928-134486195 | Common:3; Rare:91 | ||||
| chr3:136862016-136862322 | Common:1; Rare:97 | ||||
| chr3:139358780-139359084 | Common:2; Rare:70 | ||||
| chr3:139389568-139389875 | Common:2; Rare:98 |