| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186567291-186567469 | Common:3; Rare:42 | ||||
| chr3:186783209-186783594 | Common:2; Rare:148 | ||||
| chr3:186806429-186806534 | Rare:32 | ||||
| chr3:186930227-186930760 | Common:5; Rare:128 | ||||
| chr3:187025271-187025483 | Rare:29 | ||||
| chr3:187291687-187291864 | Common:1; Rare:64 | ||||
| chr3:188153762-188153950 | Common:1; Rare:37 | ||||
| chr3:188154041-188154224 | Rare:60 | ||||
| chr3:190322432-190322519 | Rare:24 | ||||
| chr3:191329267-191329697 | Common:4; Rare:130 | ||||
| chr3:192917830-192918033 | Common:2; Rare:89 | ||||
| chr3:193240987-193241327 | Common:4; Rare:116 | ||||
| chr3:193554985-193555112 | Rare:28 | ||||
| chr3:193593091-193593402 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486970-194487166 | Common:4; Rare:94 |