| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9917033-9917195 | Common:2; Rare:30 | ||||
| chr3:9933465-9933879 | Common:2; Rare:167; Clinvar:4 | ||||
| chr3:10026304-10026473 | Rare:54 | ||||
| chr3:10115515-10115712 | Common:4; Rare:70 | ||||
| chr3:11643755-11644113 | Common:3; Rare:94 | ||||
| chr3:11719427-11719595 | Rare:53 | ||||
| chr3:11846843-11846982 | Common:1; Rare:41 | ||||
| chr3:12158857-12159032 | Rare:59 | ||||
| chr3:12288817-12289067 | Common:1; Rare:49 | ||||
| chr3:12484330-12484589 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556983-12557153 | Common:4; Rare:69 | ||||
| chr3:12664060-12664330 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:12796592-12796723 | Common:3; Rare:44 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:13548974-13549169 | Common:1; Rare:60 |