| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45034690-45034869 | Common:2; Rare:35 | ||||
| chr3:48433951-48434082 | Rare:22 | ||||
| chr3:49131407-49131713 | Common:1; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:54637851-54638011 | Common:1; Rare:43 | ||||
| chr3:61560653-61560823 | Common:1; Rare:53 | ||||
| chr3:61560881-61561040 | Common:2; Rare:45 | ||||
| chr3:62150023-62150108 | Rare:14 | ||||
| chr3:64685003-64685171 | Rare:38 | ||||
| chr3:69086176-69086340 | Rare:19 | ||||
| chr3:75435060-75435395 | Common:4; Rare:117 | ||||
| chr3:75641103-75641386 | Common:1; Rare:46 | ||||
| chr3:81758982-81759025 | Rare:4 | ||||
| chr3:81761197-81761319 | Rare:39 | ||||
| chr3:101576981-101577088 | Rare:31 | ||||
| chr3:101676275-101676514 | Common:1; Rare:83 |