| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12288619-12288918 | Common:2; Rare:61 | ||||
| chr3:12288927-12289113 | Common:1; Rare:39 | ||||
| chr3:12484195-12484554 | Common:5; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664087-12664300 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13480078-13480330 | Common:1; Rare:60 | ||||
| chr3:13548982-13549181 | Common:1; Rare:66 | ||||
| chr3:14124736-14125202 | Common:4; Rare:137; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14178569-14178861 | Common:2; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402437-14402729 | Rare:67 | ||||
| chr3:14651486-14651817 | Rare:97 | ||||
| chr3:14947149-14947182 | Rare:11 | ||||
| chr3:14947192-14947569 | Common:4; Rare:165 | ||||
| chr3:14948024-14948208 | Rare:81 | ||||
| chr3:14948360-14948637 | Common:2; Rare:74 | ||||
| chr3:15032573-15032794 | Rare:42 |