| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16175512-16175529 | Rare:6 | ||||
| chr3:16264872-16265243 | Common:2; Rare:124 | ||||
| chr3:16513482-16513841 | Common:4; Rare:87 | ||||
| chr3:16884828-16885228 | Common:8; Rare:98 | ||||
| chr3:17742507-17742952 | Common:4; Rare:156 | ||||
| chr3:18424201-18424565 | Common:5; Rare:72 | ||||
| chr3:18444866-18445002 | Rare:32 | ||||
| chr3:19946974-19947450 | Common:7; Rare:177 | ||||
| chr3:19975329-19975738 | Common:1; Rare:103 | ||||
| chr3:20186182-20186500 | Common:3; Rare:100 | ||||
| chr3:23202926-23203194 | Common:1; Rare:96 | ||||
| chr3:23916878-23917181 | Rare:116 | ||||
| chr3:23917670-23918021 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr3:24494691-24494917 | Rare:58 | ||||
| chr3:25428106-25428289 | Rare:34 |