| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149086452-149086720 | Rare:79 | ||||
| chr3:149129545-149129714 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149333429-149333529 | Common:3; Rare:12 | ||||
| chr3:149333573-149333767 | Rare:39 | ||||
| chr3:149377369-149377977 | Common:1; Rare:158 | ||||
| chr3:149576207-149576480 | Rare:38 | ||||
| chr3:149657977-149658175 | Rare:43 | ||||
| chr3:149752361-149752579 | Common:2; Rare:83 | ||||
| chr3:149812564-149812767 | Common:1; Rare:56 | ||||
| chr3:149812999-149813298 | Common:2; Rare:101 | ||||
| chr3:149969261-149969467 | Common:1; Rare:54 | ||||
| chr3:149971128-149971336 | Common:3; Rare:96 | ||||
| chr3:150408004-150408320 | Common:2; Rare:94 | ||||
| chr3:150603134-150603422 | Common:2; Rare:117 | ||||
| chr3:150763522-150763615 | Rare:28 |