| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188947439-188947590 | Rare:26 | ||||
| chr3:189100030-189100182 | Common:1; Rare:21 | ||||
| chr3:190513903-190514113 | Common:2; Rare:61 | ||||
| chr3:191329304-191329659 | Common:3; Rare:107 | ||||
| chr3:192727359-192727682 | Rare:73 | ||||
| chr3:193240963-193241343 | Common:4; Rare:131 | ||||
| chr3:193593086-193593404 | Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194487008-194487166 | Common:3; Rare:70 | ||||
| chr3:195543215-195543469 | Common:3; Rare:97 | ||||
| chr3:195583881-195584078 | Rare:42 | ||||
| chr3:195584090-195584377 | Common:12; Rare:57 | ||||
| chr3:196082060-196082259 | Common:2; Rare:76 | ||||
| chr3:196287623-196287823 | Common:1; Rare:65 | ||||
| chr3:196318184-196318362 | Common:1; Rare:72 | ||||
| chr3:196568518-196568621 | Common:1; Rare:25 |