| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157174794-157175269 | Common:3; Rare:201 | ||||
| chr3:158599882-158600083 | Common:2; Rare:45 | ||||
| chr3:158689996-158690186 | Rare:37; Clinvar:1 | ||||
| chr3:158718775-158718791 | Rare:1 | ||||
| chr3:168025040-168025216 | Common:1; Rare:30 | ||||
| chr3:169764853-169765286 | Common:1; Rare:149; Clinvar:17; Clinvar (pathogenic):6 | ||||
| chr3:171874372-171874557 | Common:3; Rare:32 | ||||
| chr3:179681573-179681670 | Common:1; Rare:19 | ||||
| chr3:184332482-184332752 | Common:1; Rare:53 | ||||
| chr3:185656435-185656755 | Rare:67 | ||||
| chr3:185658515-185658918 | Common:1; Rare:78 | ||||
| chr3:186990608-186990738 | Common:1; Rare:14 | ||||
| chr3:187738847-187739141 | Common:3; Rare:62 | ||||
| chr3:187739447-187739665 | Rare:39 | ||||
| chr3:187740273-187740557 | Common:3; Rare:46 |