| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11846523-11846941 | Common:3; Rare:281 | ||||
| chr3:12287634-12288052 | Common:17; Rare:140 | ||||
| chr3:12288833-12289100 | Common:3; Rare:99 | ||||
| chr3:12484262-12484623 | Common:15; Rare:280; Clinvar:9; Clinvar (benign):6 | ||||
| chr3:12545393-12545797 | Common:5; Rare:174 | ||||
| chr3:12556812-12557218 | Common:15; Rare:313 | ||||
| chr3:12663353-12663753 | Common:14; Rare:181 | ||||
| chr3:12664007-12664480 | Common:8; Rare:297; Clinvar:3; Clinvar (benign):13 | ||||
| chr3:12759080-12759520 | Common:7; Rare:160 | ||||
| chr3:12841455-12841960 | Common:4; Rare:281 | ||||
| chr3:12967601-12968038 | Common:5; Rare:152 | ||||
| chr3:12986990-12987350 | Common:2; Rare:129 | ||||
| chr3:12994649-12994822 | Rare:24 | ||||
| chr3:12994894-12995204 | Common:2; Rare:136 | ||||
| chr3:13419691-13419881 | Common:2; Rare:47 |