| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186783225-186783610 | Common:2; Rare:162 | ||||
| chr3:186806429-186806541 | Rare:35 | ||||
| chr3:187291687-187291864 | Common:1; Rare:64 | ||||
| chr3:187670260-187670506 | Rare:57 | ||||
| chr3:188153646-188153956 | Common:1; Rare:61 | ||||
| chr3:188154060-188154215 | Rare:47 | ||||
| chr3:193593091-193593382 | Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194487003-194487166 | Common:3; Rare:73 | ||||
| chr3:195583896-195584116 | Rare:45 | ||||
| chr3:196082068-196082259 | Common:2; Rare:72 | ||||
| chr3:196318168-196318336 | Common:1; Rare:74 | ||||
| chr3:196432365-196432520 | Common:1; Rare:71 | ||||
| chr3:196503722-196503855 | Common:1; Rare:43 | ||||
| chr3:196639604-196639797 | Common:2; Rare:47 | ||||
| chr3:196712185-196712373 | Common:3; Rare:64 |