| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156674327-156674669 | Common:4; Rare:101 | ||||
| chr3:156826217-156826382 | Common:1; Rare:58 | ||||
| chr3:157159807-157160343 | Common:1; Rare:196 | ||||
| chr3:157543201-157543427 | Common:1; Rare:50 | ||||
| chr3:158105726-158105878 | Common:5; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158571054-158571282 | Common:1; Rare:69 | ||||
| chr3:158672545-158672731 | Common:2; Rare:53 | ||||
| chr3:158732153-158732318 | Common:6; Rare:50 | ||||
| chr3:158732752-158732944 | Rare:25 | ||||
| chr3:158801976-158802234 | Common:3; Rare:114 | ||||
| chr3:159763632-159763721 | Rare:27 | ||||
| chr3:159764282-159764562 | Common:2; Rare:80 | ||||
| chr3:159853109-159853307 | Rare:38 | ||||
| chr3:160399156-160399669 | Rare:139; Clinvar:7 | ||||
| chr3:160449743-160449874 | Common:1; Rare:46 |