| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142578685-142578976 | Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596264-142596451 | Common:2; Rare:50 | ||||
| chr3:142723901-142724053 | Rare:46 | ||||
| chr3:143001319-143001631 | Common:5; Rare:100 | ||||
| chr3:143971711-143971845 | Common:1; Rare:63 | ||||
| chr3:143971961-143972074 | Rare:43 | ||||
| chr3:146160961-146161276 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146544514-146544831 | Common:4; Rare:74 | ||||
| chr3:149086452-149086731 | Rare:83 | ||||
| chr3:149129549-149129718 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149752257-149752610 | Common:2; Rare:133 | ||||
| chr3:149813065-149813265 | Common:1; Rare:69 | ||||
| chr3:149969378-149969457 | Common:1; Rare:20 | ||||
| chr3:149971125-149971366 | Common:3; Rare:117 | ||||
| chr3:150408160-150408302 | Common:1; Rare:57 |