| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12484319-12484554 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556741-12557153 | Common:5; Rare:113 | ||||
| chr3:12663812-12663971 | Rare:45; Clinvar:4; Clinvar (benign):3 | ||||
| chr3:12664011-12664351 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:12967664-12967972 | Common:4; Rare:111 | ||||
| chr3:13480040-13480428 | Common:3; Rare:89 | ||||
| chr3:14124690-14125133 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178467-14178870 | Common:3; Rare:194; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402461-14402756 | Common:3; Rare:64 | ||||
| chr3:14651400-14651844 | Common:1; Rare:138 | ||||
| chr3:14947086-14947361 | Common:2; Rare:100 | ||||
| chr3:14947381-14947602 | Common:3; Rare:103 | ||||
| chr3:14948255-14948708 | Common:2; Rare:161 | ||||
| chr3:15099119-15099286 | Rare:39 | ||||
| chr3:15427447-15427657 | Common:1; Rare:74 |