| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9986786-9986938 | Common:2; Rare:57 | ||||
| chr3:10011070-10011430 | Common:1; Rare:99 | ||||
| chr3:10026329-10026489 | Rare:45 | ||||
| chr3:10115475-10115739 | Common:4; Rare:99 | ||||
| chr3:10141650-10141886 | Common:3; Rare:107; Clinvar:21; Clinvar (benign):20 | ||||
| chr3:10248241-10248562 | Common:5; Rare:102 | ||||
| chr3:10249013-10249547 | Common:11; Rare:357 | ||||
| chr3:10321038-10321288 | Common:2; Rare:99 | ||||
| chr3:11272202-11272478 | Common:4; Rare:71 | ||||
| chr3:11643468-11643720 | Common:2; Rare:47 | ||||
| chr3:11643780-11644104 | Common:3; Rare:86 | ||||
| chr3:11719352-11719752 | Rare:167 | ||||
| chr3:11720407-11720807 | Common:2; Rare:132 | ||||
| chr3:11846815-11847039 | Common:1; Rare:65 | ||||
| chr3:12484182-12484556 | Common:5; Rare:112; Clinvar:3; Clinvar (benign):2 |