| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123601832-123602144 | Common:6; Rare:80 | ||||
| chr12:123633632-123633864 | Common:2; Rare:109; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972573-123972887 | Common:6; Rare:111 | ||||
| chr12:130871730-130872104 | Common:4; Rare:157 | ||||
| chr12:131710779-131711125 | Rare:98 | ||||
| chr12:132687322-132687713 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):8 | ||||
| chr12:132887558-132887845 | Rare:82 | ||||
| chr12:132956280-132956435 | Common:1; Rare:30 | ||||
| chr12:132986263-132986433 | Rare:37 | ||||
| chr12:133130218-133130662 | Common:7; Rare:150 | ||||
| chr13:19633385-19633735 | Common:1; Rare:134 | ||||
| chr13:19782907-19783088 | Common:2; Rare:66 | ||||
| chr13:19863538-19863866 | Common:5; Rare:121 | ||||
| chr13:21176484-21176713 | Common:2; Rare:102 | ||||
| chr13:21459194-21459513 | Common:1; Rare:113 |