| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131949675-131949971 | Common:2; Rare:93 | ||||
| chr12:132687294-132687707 | Common:4; Rare:156; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887553-132887845 | Rare:85 | ||||
| chr12:132956254-132956410 | Common:1; Rare:36 | ||||
| chr12:132986274-132986460 | Rare:48 | ||||
| chr12:133037220-133037536 | Common:4; Rare:64 | ||||
| chr12:133130249-133130573 | Common:6; Rare:101 | ||||
| chr13:19863440-19863870 | Common:5; Rare:148 | ||||
| chr13:20525791-20525941 | Common:1; Rare:64 | ||||
| chr13:21140390-21140636 | Rare:112 | ||||
| chr13:21176484-21176711 | Common:2; Rare:101 | ||||
| chr13:23579216-23579488 | Common:5; Rare:85 | ||||
| chr13:23889294-23889477 | Rare:68 | ||||
| chr13:24160558-24160764 | Rare:59 | ||||
| chr13:24512723-24512856 | Common:3; Rare:38 |