| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157543204-157543427 | Common:1; Rare:50 | ||||
| chr3:158105726-158105893 | Common:5; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158110011-158110194 | Rare:44 | ||||
| chr3:158672550-158672716 | Common:2; Rare:48 | ||||
| chr3:158732165-158732341 | Common:6; Rare:51 | ||||
| chr3:158801967-158802228 | Common:3; Rare:117 | ||||
| chr3:158819495-158819709 | Common:5; Rare:58 | ||||
| chr3:159763180-159763340 | Rare:29 | ||||
| chr3:159763632-159763698 | Rare:21 | ||||
| chr3:159764328-159764389 | Common:1; Rare:14 | ||||
| chr3:160399196-160399295 | Rare:25; Clinvar:1 | ||||
| chr3:160399403-160399693 | Rare:79; Clinvar:3 | ||||
| chr3:160449743-160449892 | Common:1; Rare:47 | ||||
| chr3:160565271-160565520 | Common:1; Rare:74 | ||||
| chr3:160565528-160565843 | Common:2; Rare:116 |