| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601823-15602010 | Common:1; Rare:94; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:15859777-15860127 | Common:4; Rare:112 | ||||
| chr3:16174047-16174267 | Common:3; Rare:37 | ||||
| chr3:16264864-16265262 | Common:2; Rare:136 | ||||
| chr3:16265278-16265459 | Rare:34 | ||||
| chr3:16512833-16512980 | Common:1; Rare:30 | ||||
| chr3:16513044-16513061 | Rare:4 | ||||
| chr3:16513275-16513793 | Common:4; Rare:144 | ||||
| chr3:16513909-16514037 | Rare:22 | ||||
| chr3:16884922-16885217 | Common:7; Rare:87 | ||||
| chr3:17742507-17742952 | Common:4; Rare:156 | ||||
| chr3:18424230-18424568 | Common:6; Rare:70 | ||||
| chr3:19946974-19947462 | Common:7; Rare:181 | ||||
| chr3:20039924-20040066 | Common:1; Rare:34 | ||||
| chr3:20186176-20186421 | Common:2; Rare:78 |