| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28241441-28241777 | Common:2; Rare:114 | ||||
| chr3:28348779-28348874 | Common:1; Rare:28 | ||||
| chr3:28348994-28349170 | Common:2; Rare:50 | ||||
| chr3:31981634-31981788 | Common:1; Rare:40 | ||||
| chr3:32391673-32391961 | Common:4; Rare:83 | ||||
| chr3:32570655-32570920 | Rare:125 | ||||
| chr3:33097090-33097258 | Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277295-33277476 | Common:2; Rare:45 | ||||
| chr3:33717998-33718308 | Rare:113 | ||||
| chr3:33798520-33798860 | Common:3; Rare:114 | ||||
| chr3:36993117-36993563 | Common:2; Rare:139; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37065823-37066085 | Common:2; Rare:64 | ||||
| chr3:37243122-37243420 | Common:3; Rare:78 | ||||
| chr3:37861746-37861862 | Rare:25 | ||||
| chr3:38029600-38029844 | Common:1; Rare:49 |