| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123584289-123584629 | Common:6; Rare:120 | ||||
| chr12:123633617-123633851 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972587-123972893 | Common:6; Rare:106 | ||||
| chr12:132687322-132687707 | Common:4; Rare:140; Clinvar:2; Clinvar (benign):8 | ||||
| chr12:132887553-132887810 | Rare:79 | ||||
| chr12:132956280-132956423 | Common:1; Rare:28 | ||||
| chr12:132986236-132986442 | Rare:46 | ||||
| chr12:133130232-133130652 | Common:7; Rare:139 | ||||
| chr13:19633472-19633751 | Common:1; Rare:109 | ||||
| chr13:19958519-19958846 | Common:6; Rare:149 | ||||
| chr13:20525801-20525936 | Common:1; Rare:58 | ||||
| chr13:21140377-21140622 | Rare:111 | ||||
| chr13:21176466-21176708 | Common:2; Rare:105 | ||||
| chr13:23570293-23570495 | Common:1; Rare:42 | ||||
| chr13:23570606-23570835 | Common:1; Rare:47 |