| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149657973-149658212 | Rare:54 | ||||
| chr3:149812584-149812745 | Common:1; Rare:45 | ||||
| chr3:149813087-149813291 | Common:1; Rare:73 | ||||
| chr3:150408090-150408320 | Common:2; Rare:79 | ||||
| chr3:150603145-150603389 | Common:2; Rare:95 | ||||
| chr3:152268738-152269086 | Rare:131 | ||||
| chr3:152269544-152269689 | Rare:38 | ||||
| chr3:154121334-154121457 | Common:3; Rare:56 | ||||
| chr3:155854364-155854721 | Rare:102 | ||||
| chr3:156674353-156674656 | Common:3; Rare:91 | ||||
| chr3:156826140-156826307 | Common:3; Rare:52 | ||||
| chr3:157160083-157160327 | Rare:102 | ||||
| chr3:158105739-158105869 | Common:5; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158801997-158802152 | Common:2; Rare:73 | ||||
| chr3:160399196-160399312 | Rare:32; Clinvar:1 |