| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792685-9793123 | Common:3; Rare:155 | ||||
| chr3:9986778-9987177 | Common:3; Rare:114 | ||||
| chr3:10026334-10026459 | Rare:36 | ||||
| chr3:10115522-10115712 | Common:3; Rare:69 | ||||
| chr3:11154375-11154511 | Common:3; Rare:38 | ||||
| chr3:11225898-11225985 | Rare:11 | ||||
| chr3:12664087-12664274 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13480073-13480339 | Common:1; Rare:63 | ||||
| chr3:13548990-13549173 | Common:1; Rare:60 | ||||
| chr3:14124728-14125184 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178870 | Common:2; Rare:160; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14948033-14948208 | Rare:75 | ||||
| chr3:15065233-15065596 | Common:5; Rare:103 | ||||
| chr3:15206019-15206269 | Rare:90 | ||||
| chr3:15427471-15427629 | Common:1; Rare:57 |