| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792736-9793127 | Common:3; Rare:133 | ||||
| chr3:10026304-10026446 | Rare:48 | ||||
| chr3:10115641-10115784 | Common:2; Rare:50 | ||||
| chr3:10164703-10164945 | Common:2; Rare:76 | ||||
| chr3:11225834-11226020 | Rare:30 | ||||
| chr3:14124713-14125152 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178566-14178857 | Common:2; Rare:152; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14947343-14947583 | Common:3; Rare:111 | ||||
| chr3:15427495-15427629 | Rare:47 | ||||
| chr3:15601478-15601803 | Common:4; Rare:137; Clinvar:1 | ||||
| chr3:16264869-16265237 | Common:2; Rare:125 | ||||
| chr3:16513600-16513865 | Common:4; Rare:72 | ||||
| chr3:19946980-19947214 | Common:4; Rare:84 | ||||
| chr3:23916919-23917214 | Rare:111 | ||||
| chr3:29280825-29281076 | Common:3; Rare:50 |