| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158110328-158110412 | Common:1; Rare:19 | ||||
| chr3:158571084-158571240 | Rare:54 | ||||
| chr3:158801812-158802201 | Common:3; Rare:134 | ||||
| chr3:159763170-159763348 | Rare:32 | ||||
| chr3:159764323-159764488 | Common:1; Rare:44 | ||||
| chr3:159852997-159853090 | Rare:10 | ||||
| chr3:159853113-159853270 | Rare:34 | ||||
| chr3:160399196-160399310 | Rare:31; Clinvar:1 | ||||
| chr3:160399492-160399726 | Rare:69; Clinvar:1 | ||||
| chr3:160402513-160402867 | Common:1; Rare:77 | ||||
| chr3:160449500-160449645 | Rare:27 | ||||
| chr3:160565271-160565842 | Common:3; Rare:191 | ||||
| chr3:160566077-160566388 | Rare:54 | ||||
| chr3:161221196-161221388 | Common:2; Rare:61 | ||||
| chr3:167734804-167735198 | Common:2; Rare:128; Clinvar:1; Clinvar (benign):1 |