| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150763450-150763610 | Rare:39 | ||||
| chr3:152268593-152269153 | Common:2; Rare:206 | ||||
| chr3:152269241-152269335 | Rare:30 | ||||
| chr3:152269532-152269689 | Rare:42 | ||||
| chr3:152299116-152299205 | Common:1; Rare:27 | ||||
| chr3:152835020-152835153 | Common:2; Rare:49 | ||||
| chr3:154121231-154121444 | Common:2; Rare:90 | ||||
| chr3:155854364-155854815 | Rare:130 | ||||
| chr3:155870317-155870743 | Common:2; Rare:122 | ||||
| chr3:156674364-156674653 | Common:3; Rare:84 | ||||
| chr3:156826154-156826381 | Common:3; Rare:76 | ||||
| chr3:157153469-157153566 | Rare:19 | ||||
| chr3:157159807-157159896 | Rare:20 | ||||
| chr3:157159997-157160343 | Rare:142 | ||||
| chr3:158105732-158105887 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):1 |