| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156674362-156674618 | Common:3; Rare:73 | ||||
| chr3:156826217-156826331 | Common:1; Rare:41 | ||||
| chr3:157160069-157160261 | Rare:80 | ||||
| chr3:158105739-158105883 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158801984-158802146 | Common:2; Rare:78 | ||||
| chr3:159852997-159853315 | Rare:55 | ||||
| chr3:160399177-160399309 | Rare:35; Clinvar:2 | ||||
| chr3:160399518-160399693 | Rare:40 | ||||
| chr3:160449748-160449859 | Rare:40 | ||||
| chr3:160565517-160565842 | Common:2; Rare:117 | ||||
| chr3:161105277-161105384 | Common:2; Rare:36 | ||||
| chr3:167734839-167735198 | Common:2; Rare:111; Clinvar (benign):1 | ||||
| chr3:169773287-169773424 | Rare:51 | ||||
| chr3:170870163-170870304 | Rare:74 | ||||
| chr3:172523391-172523507 | Common:1; Rare:31 |