| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:187291880-187291903 | Rare:6 | ||||
| chr3:187292000-187292318 | Common:15; Rare:62 | ||||
| chr3:187737901-187738136 | Common:2; Rare:43 | ||||
| chr3:188153785-188154021 | Common:1; Rare:42 | ||||
| chr3:188154060-188154232 | Rare:58 | ||||
| chr3:190322213-190322552 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr3:190513872-190514177 | Common:2; Rare:78 | ||||
| chr3:190615123-190615337 | Common:1; Rare:36 | ||||
| chr3:190862614-190862782 | Rare:50 | ||||
| chr3:191329333-191329638 | Common:3; Rare:88 | ||||
| chr3:192917838-192918008 | Common:2; Rare:76 | ||||
| chr3:193593088-193593380 | Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194351256-194351505 | Common:2; Rare:39 | ||||
| chr3:194486966-194487150 | Common:4; Rare:91 | ||||
| chr3:195443086-195443380 | Common:3; Rare:87 |