| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132828831-132828888 | Common:1; Rare:26 | ||||
| chr12:132887555-132887908 | Rare:100 | ||||
| chr12:132956271-132956386 | Common:1; Rare:28 | ||||
| chr12:132986247-132986428 | Rare:39 | ||||
| chr12:133037474-133037536 | Rare:15 | ||||
| chr12:133080733-133080934 | Rare:63 | ||||
| chr12:133130238-133130522 | Common:6; Rare:85 | ||||
| chr13:19633454-19633727 | Common:1; Rare:104 | ||||
| chr13:19782918-19783088 | Common:2; Rare:62 | ||||
| chr13:19958468-19958751 | Common:5; Rare:137 | ||||
| chr13:21140377-21140624 | Rare:111 | ||||
| chr13:21176473-21176713 | Common:2; Rare:107 | ||||
| chr13:21459266-21459568 | Common:2; Rare:110 | ||||
| chr13:21603855-21603923 | Rare:33 | ||||
| chr13:21670896-21671162 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 |